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Osteomyelitis

MedGen UID:
10497
Concept ID:
C0029443
Disease or Syndrome
Synonyms: Bone infection
SNOMED CT: OSTM - Osteomyelitis (60168000); OM - Osteomyelitis (60168000); Osteomyelitis (60168000); Pyogenic inflammation of bone (60168000)
 
HPO: HP:0002754

Conditions with this feature

Hb SS disease
MedGen UID:
287
Concept ID:
C0002895
Disease or Syndrome
Sickle cell disease (SCD) is characterized by intermittent vaso-occlusive events and chronic hemolytic anemia. Vaso-occlusive events result in tissue ischemia leading to acute and chronic pain as well as organ damage that can affect any organ system, including the bones, spleen, liver, brain, lungs, kidneys, and joints. Dactylitis (pain and/or swelling of the hands or feet) is often the earliest manifestation of SCD. In children, the spleen can become engorged with blood cells in a “splenic sequestration.” The spleen is particularly vulnerable to infarction and the majority of individuals with SCD who are not on hydroxyurea or transfusion therapy become functionally asplenic in early childhood, increasing their risk for certain types of bacterial infections. Acute chest syndrome is a major cause of mortality in SCD. Chronic hemolysis can result in varying degrees of anemia, jaundice, cholelithiasis, and delayed growth and sexual maturation. Individuals with the highest rates of hemolysis are predisposed to pulmonary artery hypertension, priapism, and leg ulcers but may be relatively protected from vaso-occlusive pain.
beta Thalassemia
MedGen UID:
2611
Concept ID:
C0005283
Disease or Syndrome
Beta-thalassemia (ß-thalassemia) is characterized by reduced synthesis of the hemoglobin subunit beta (hemoglobin beta chain) that results in microcytic hypochromic anemia, an abnormal peripheral blood smear with nucleated red blood cells, and reduced amounts of hemoglobin A (HbA) on hemoglobin analysis. Individuals with thalassemia major have severe anemia and hepatosplenomegaly; they usually come to medical attention within the first two years of life. Without treatment, affected children have severe failure to thrive and shortened life expectancy. Treatment with a regular transfusion program and chelation therapy, aimed at reducing transfusion iron overload, allows for normal growth and development and may improve the overall prognosis. Individuals with thalassemia intermedia present later and have milder anemia that does not require regular treatment with blood transfusion. These individuals are at risk for iron overload secondary to increased intestinal absorption of iron as a result of ineffective erythropoiesis.
Hereditary persistence of fetal hemoglobin
MedGen UID:
5495
Concept ID:
C0019025
Disease or Syndrome
The persistence of substantial fetal hemoglobin production into adulthood, usually associated with hemoglobinopathies due to mutations in the alpha and/or beta chain of hemoglobin.
Hereditary insensitivity to pain with anhidrosis
MedGen UID:
6915
Concept ID:
C0020074
Disease or Syndrome
Congenital insensitivity to pain with anhidrosis (CIPA), also known as hereditary sensory and autonomic neuropathy type IV (HSAN IV), is characterized by insensitivity to pain, anhidrosis (the inability to sweat), and intellectual disability. The ability to sense all pain (including visceral pain) is absent, resulting in repeated injuries including: oral self-mutilation (biting of tongue, lips, and buccal mucosa); biting of fingertips; bruising, scarring, and infection of the skin; multiple bone fractures (many of which fail to heal properly); and recurrent joint dislocations resulting in joint deformity. Sense of touch, vibration, and position are normal. Anhidrosis predisposes to recurrent febrile episodes that are often the initial manifestation of CIPA. Hypothermia in cold environments also occurs. Intellectual disability of varying degree is observed in most affected individuals; hyperactivity and emotional lability are common.
Fanconi-like syndrome
MedGen UID:
56237
Concept ID:
C0151638
Disease or Syndrome
Thalassemia intermedia
MedGen UID:
82892
Concept ID:
C0271979
Disease or Syndrome
beta^0^ Thalassemia
MedGen UID:
506753
Concept ID:
C0271980
Disease or Syndrome
Delta-beta thalassemia
MedGen UID:
78790
Concept ID:
C0271985
Disease or Syndrome
Beta thalassemia intermedia
MedGen UID:
450544
Concept ID:
C0472767
Disease or Syndrome
Methemoglobinemia, beta-globin type
MedGen UID:
333645
Concept ID:
C1840779
Disease or Syndrome
Methemoglobinemia, beta-globin type is a condition that affects the function of red blood cells. Specifically, it alters a molecule called hemoglobin within these cells. Hemoglobin within red blood cells attaches (binds) to oxygen molecules in the lungs, which it carries through the bloodstream, then releases in tissues throughout the body. Instead of normal hemoglobin, people with methemoglobinemia, beta-globin type have an abnormal form called methemoglobin, which is unable to efficiently deliver oxygen to the body's tissues. In methemoglobinemia, beta-globin type, the abnormal hemoglobin gives the blood a brown color. It also causes a bluish appearance of the skin, lips, and nails (cyanosis), which usually first appears around the age of 6 months. The signs and symptoms of methemoglobinemia, beta-globin type are generally limited to cyanosis, which does not cause any health problems. However, in rare cases, severe methemoglobinemia, beta-globin type can cause headaches, weakness, and fatigue.
Erythremia, Beta-Globin Type
MedGen UID:
327189
Concept ID:
C1840780
Disease or Syndrome
Immunodeficiency with hyper IgM type 4
MedGen UID:
330847
Concept ID:
C1842413
Disease or Syndrome
Hyper-IgM syndrome is a condition characterized by normal or increased serum IgM concentrations associated with low or absent serum IgG, IgA, and IgE concentrations, indicating a defect in the class-switch recombination (CSR) process (summary by Imai et al., 2003). For a discussion of genetic heterogeneity of immunodeficiency with hyper-IgM, see HIGM1 (308230).
Chronic granulomatous disease, X-linked
MedGen UID:
336165
Concept ID:
C1844376
Disease or Syndrome
Chronic granulomatous disease (CGD) is a primary immunodeficiency disorder of phagocytes (neutrophils, monocytes, macrophages, and eosinophils) resulting from impaired killing of bacteria and fungi. CGD is characterized by severe recurrent bacterial and fungal infections and dysregulated inflammatory response resulting in granuloma formation and other inflammatory disorders such as colitis. Infections typically involve the lung (pneumonia), lymph nodes (lymphadenitis), liver (abscess), bone (osteomyelitis), and skin (abscesses or cellulitis); granulomas typically involve the genitourinary system (bladder) and gastrointestinal tract (often the pylorus initially, and later the esophagus, jejunum, ileum, cecum, rectum, and perirectal area). Some males with X-linked CGD have McLeod neuroacanthocytosis syndrome as the result of a contiguous gene deletion. CGD may present any time from infancy to late adulthood; however, the vast majority of affected individuals are diagnosed before age five years. Use of antimicrobial prophylaxis and therapy has greatly improved overall survival.
Osteopetrosis autosomal recessive 1
MedGen UID:
376708
Concept ID:
C1850127
Disease or Syndrome
Osteopetrosis (OPT) is a life-threatening disease caused by subnormal osteoclast function, with an incidence of 1 in 250,000 births. The disease usually manifests in the first few months of life with macrocephaly and frontal bossing, resulting in a characteristic facial appearance. Defective bone remodeling of the skull results in choanal stenosis with concomitant respiratory problems and feeding difficulties, which are the first clinical manifestation of disease. The expanding bone encroaches on neural foramina, leading to blindness, deafness, and facial palsy. Complete visual loss invariably occurs in all untreated patients, and hearing loss is estimated to affect 78% of patients with OPT. Tooth eruption defects and severe dental caries are common. Calcium feedback hemostasis is impaired, and children with OPT are at risk of developing hypocalcemia with attendant tetanic seizures and secondary hyperparathyroidism. The most severe complication of OPT, limiting survival, is bone marrow insufficiency. The abnormal expansion of cortical and trabecular bone physically limits the availability of medullary space for hematopoietic activity, leading to life-threatening cytopenia and secondary expansion of extramedullary hematopoiesis at sites such as the liver and spleen (summary by Aker et al., 2012). Genetic Heterogeneity of Autosomal Recessive Osteopetrosis Other forms of autosomal recessive infantile malignant osteopetrosis include OPTB4 (611490), which is caused by mutation in the CLCN7 gene (602727) on chromosome 16p13, and OPTB5 (259720), which is caused by mutation in the OSTM1 gene (607649) on chromosome 6q21. A milder, osteoclast-poor form of autosomal recessive osteopetrosis (OPTB2; 259710) is caused by mutation in the TNFSF11 gene (602642) on chromosome 13q14, an intermediate form (OPTB6; 611497) is caused by mutation in the PLEKHM1 gene (611466) on chromosome 17q21, and a severe osteoclast-poor form associated with hypogammaglobulinemia (OPTB7; 612301) is caused by mutation in the TNFRSF11A gene (603499) on chromosome 18q22.1. Another form of autosomal recessive osteopetrosis (OPTB8; 615085) is caused by mutation in the SNX10 gene (614780) on chromosome 7p15. A form of autosomal recessive osteopetrosis associated with renal tubular acidosis (OPTB3; 259730) is caused by mutation in the gene encoding carbonic anhydrase II (611492) on chromosome 8q22. Autosomal dominant forms of osteopetrosis are more benign (see OPTA1, 607634). Osteosclerosis also occurs in pycnodysostosis (265800), in van Buchem disease (239100), and in sclerosteosis (269500).
Cervical hypertrichosis neuropathy
MedGen UID:
341004
Concept ID:
C1855902
Disease or Syndrome
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 2
MedGen UID:
383869
Concept ID:
C1856245
Disease or Syndrome
Chronic granulomatous disease (CGD) is a primary immunodeficiency disorder of phagocytes (neutrophils, monocytes, macrophages, and eosinophils) resulting from impaired killing of bacteria and fungi. CGD is characterized by severe recurrent bacterial and fungal infections and dysregulated inflammatory response resulting in granuloma formation and other inflammatory disorders such as colitis. Infections typically involve the lung (pneumonia), lymph nodes (lymphadenitis), liver (abscess), bone (osteomyelitis), and skin (abscesses or cellulitis); granulomas typically involve the genitourinary system (bladder) and gastrointestinal tract (often the pylorus initially, and later the esophagus, jejunum, ileum, cecum, rectum, and perirectal area). Some males with X-linked CGD have McLeod neuroacanthocytosis syndrome as the result of a contiguous gene deletion. CGD may present any time from infancy to late adulthood; however, the vast majority of affected individuals are diagnosed before age five years. Use of antimicrobial prophylaxis and therapy has greatly improved overall survival.
Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type 1
MedGen UID:
341102
Concept ID:
C1856251
Disease or Syndrome
Chronic granulomatous disease (CGD) is a primary immunodeficiency disorder of phagocytes (neutrophils, monocytes, macrophages, and eosinophils) resulting from impaired killing of bacteria and fungi. CGD is characterized by severe recurrent bacterial and fungal infections and dysregulated inflammatory response resulting in granuloma formation and other inflammatory disorders such as colitis. Infections typically involve the lung (pneumonia), lymph nodes (lymphadenitis), liver (abscess), bone (osteomyelitis), and skin (abscesses or cellulitis); granulomas typically involve the genitourinary system (bladder) and gastrointestinal tract (often the pylorus initially, and later the esophagus, jejunum, ileum, cecum, rectum, and perirectal area). Some males with X-linked CGD have McLeod neuroacanthocytosis syndrome as the result of a contiguous gene deletion. CGD may present any time from infancy to late adulthood; however, the vast majority of affected individuals are diagnosed before age five years. Use of antimicrobial prophylaxis and therapy has greatly improved overall survival.
Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
MedGen UID:
383872
Concept ID:
C1856255
Disease or Syndrome
Chronic granulomatous disease (CGD) is a primary immunodeficiency disorder of phagocytes (neutrophils, monocytes, macrophages, and eosinophils) resulting from impaired killing of bacteria and fungi. CGD is characterized by severe recurrent bacterial and fungal infections and dysregulated inflammatory response resulting in granuloma formation and other inflammatory disorders such as colitis. Infections typically involve the lung (pneumonia), lymph nodes (lymphadenitis), liver (abscess), bone (osteomyelitis), and skin (abscesses or cellulitis); granulomas typically involve the genitourinary system (bladder) and gastrointestinal tract (often the pylorus initially, and later the esophagus, jejunum, ileum, cecum, rectum, and perirectal area). Some males with X-linked CGD have McLeod neuroacanthocytosis syndrome as the result of a contiguous gene deletion. CGD may present any time from infancy to late adulthood; however, the vast majority of affected individuals are diagnosed before age five years. Use of antimicrobial prophylaxis and therapy has greatly improved overall survival.
Beta-thalassemia, dominant inclusion body type
MedGen UID:
347036
Concept ID:
C1858990
Disease or Syndrome
Beta thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the iron-containing protein in red blood cells that carries oxygen to cells throughout the body.In people with beta thalassemia, low levels of hemoglobin lead to a lack of oxygen in many parts of the body. Affected individuals also have a shortage of red blood cells (anemia), which can cause pale skin, weakness, fatigue, and more serious complications. People with beta thalassemia are at an increased risk of developing abnormal blood clots.Beta thalassemia is classified into two types depending on the severity of symptoms: thalassemia major (also known as Cooley's anemia) and thalassemia intermedia. Of the two types, thalassemia major is more severe.The signs and symptoms of thalassemia major appear within the first 2 years of life. Children develop life-threatening anemia. They do not gain weight and grow at the expected rate (failure to thrive) and may develop yellowing of the skin and whites of the eyes (jaundice). Affected individuals may have an enlarged spleen, liver, and heart, and their bones may be misshapen. Some adolescents with thalassemia major experience delayed puberty. Many people with thalassemia major have such severe symptoms that they need frequent blood transfusions to replenish their red blood cell supply. Over time, an influx of iron-containing hemoglobin from chronic blood transfusions can lead to a buildup of iron in the body, resulting in liver, heart, and hormone problems.Thalassemia intermedia is milder than thalassemia major. The signs and symptoms of thalassemia intermedia appear in early childhood or later in life. Affected individuals have mild to moderate anemia and may also have slow growth and bone abnormalities.
Majeed syndrome
MedGen UID:
351273
Concept ID:
C1864997
Disease or Syndrome
Majeed syndrome is characterized by: Chronic recurrent multifocal osteomyelitis (CRMO) that is of early onset with a lifelong course; and Congenital dyserythropoietic anemia (CDA) that presents as hypochromic, microcytic anemia during the first year of life and ranges from mild to transfusion dependent. Some individuals also develop a transient inflammatory dermatosis, often manifesting as Sweet syndrome (neutrophilic skin infiltration).
Malaria, resistance to
MedGen UID:
404075
Concept ID:
C2720293
Finding
Osteomyelitis, sterile multifocal, with periostitis and pustulosis
MedGen UID:
411230
Concept ID:
C2748507
Disease or Syndrome
Hereditary sensory and autonomic neuropathy type IIB
MedGen UID:
413474
Concept ID:
C2751092
Disease or Syndrome
Hereditary sensory and autonomic neuropathy type II (HSAN2) is characterized by progressively reduced sensation to pain, temperature, and touch. Onset can be at birth and is often before puberty. The sensory deficit is predominantly distal with the lower limbs more severely affected than the upper limbs. Over time sensory function becomes severely reduced. Unnoticed injuries and neuropathic skin promote ulcerations and infections that result in spontaneous amputation of digits or the need for surgical amputation. Osteomyelitis is common. Painless fractures can complicate the disease. Autonomic disturbances are variable and can include hyperhidrosis, tonic pupils, and urinary incontinence in those with more advanced disease.
Hereditary sensory and autonomic neuropathy type IC
MedGen UID:
462246
Concept ID:
C3150896
Disease or Syndrome
Hereditary sensory neuropathy type IE
MedGen UID:
481515
Concept ID:
C3279885
Disease or Syndrome
DNMT1 -related dementia, deafness, and sensory neuropathy (HSAN IE) is a degenerative disorder of the central and peripheral nervous systems characterized by sensory impairment of the distal lower extremities, loss of sweating (sudomotor function) on the distal aspects of the upper and lower limbs, sensorineural hearing loss, and dementia. Affected persons are normal in their youth but begin to manifest progressive sensory neuropathy and moderate to severe progressive sensorineural deafness by age 20 to 35 years. The sensory alterations result in gait unsteadiness from sensory ataxia and mutilating ulcers and/or amputations of distal extremities in approximately 50% of affected persons. Dementia usually manifests by the fourth decade.
Hereditary sensory neuropathy type IF
MedGen UID:
816524
Concept ID:
C3810194
Disease or Syndrome
Hereditary sensory neuropathy type IF is an autosomal dominant sensory neuropathy affecting the lower limbs. Distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation. There is no autonomic involvement, spasticity, or cognitive impairment (summary by Kornak et al., 2014). For a discussion of genetic heterogeneity of HSN, see HSAN1A (162400).
Beta-plus-thalassemia
MedGen UID:
854234
Concept ID:
C3841475
Disease or Syndrome
HEMOGLOBIN PASADENA
MedGen UID:
854734
Concept ID:
C3888032
Finding
HEMOGLOBIN PERTH
MedGen UID:
854754
Concept ID:
C3888084
Finding
HEMOGLOBIN S
MedGen UID:
854851
Concept ID:
C3888302
Finding
HEMOGLOBIN BEOGRAD
MedGen UID:
854993
Concept ID:
C3889294
Finding
HEMOGLOBIN BETH ISRAEL
MedGen UID:
854994
Concept ID:
C3889295
Finding
HEMOGLOBIN BETHESDA
MedGen UID:
854995
Concept ID:
C3889296
Finding
HEMOGLOBIN BICETRE
MedGen UID:
854997
Concept ID:
C3889298
Finding
HEMOGLOBIN BOLOGNA
MedGen UID:
854999
Concept ID:
C3889300
Finding
HEMOGLOBIN BORAS
MedGen UID:
855000
Concept ID:
C3889301
Finding
HEMOGLOBIN BOUGARDIREY-MALI
MedGen UID:
855001
Concept ID:
C3889302
Finding
HEMOGLOBIN BREST
MedGen UID:
855003
Concept ID:
C3889304
Finding
HEMOGLOBIN BRIGHAM
MedGen UID:
855004
Concept ID:
C3889305
Finding
HEMOGLOBIN BRISBANE
MedGen UID:
855005
Concept ID:
C3889306
Finding
HEMOGLOBIN BRISTOL
MedGen UID:
855006
Concept ID:
C3889307
Finding
HEMOGLOBIN BRITISH COLUMBIA
MedGen UID:
855007
Concept ID:
C3889308
Finding
HEMOGLOBIN BROCKTON
MedGen UID:
855008
Concept ID:
C3889309
Finding
HEMOGLOBIN COWTOWN
MedGen UID:
855009
Concept ID:
C3889310
Finding
HEMOGLOBIN CRANSTON
MedGen UID:
855010
Concept ID:
C3889311
Finding
HEMOGLOBIN CRETE
MedGen UID:
855011
Concept ID:
C3889312
Finding
HEMOGLOBIN CRETEIL
MedGen UID:
855012
Concept ID:
C3889313
Finding
HEMOGLOBIN D (BUSHMAN)
MedGen UID:
855013
Concept ID:
C3889314
Finding
HEMOGLOBIN D (GRANADA)
MedGen UID:
855014
Concept ID:
C3889315
Finding
HEMOGLOBIN D (IBADAN)
MedGen UID:
855015
Concept ID:
C3889316
Finding
HEMOGLOBIN D (IRAN)
MedGen UID:
855016
Concept ID:
C3889317
Finding
HEMOGLOBIN D (OULED RABAH)
MedGen UID:
855017
Concept ID:
C3889318
Finding
HEMOGLOBIN D (PUNJAB)
MedGen UID:
855018
Concept ID:
C3889319
Finding
HEMOGLOBIN DEER LODGE
MedGen UID:
855019
Concept ID:
C3889320
Finding
HEMOGLOBIN DETROIT
MedGen UID:
855020
Concept ID:
C3889321
Finding
HEMOGLOBIN DJELFA
MedGen UID:
855021
Concept ID:
C3889322
Finding
HEMOGLOBIN DOHA
MedGen UID:
855022
Concept ID:
C3889323
Finding
HEMOGLOBIN DUARTE
MedGen UID:
855023
Concept ID:
C3889324
Finding
HEMOGLOBIN E
MedGen UID:
855024
Concept ID:
C3889325
Finding
HEMOGLOBIN E (SASKATOON)
MedGen UID:
855025
Concept ID:
C3889326
Finding
HEMOGLOBIN EDMONTON
MedGen UID:
855026
Concept ID:
C3889327
Finding
HEMOGLOBIN EXTREMADURA
MedGen UID:
855027
Concept ID:
C3889328
Finding
HEMOGLOBIN FANNIN-LUBBOCK
MedGen UID:
855028
Concept ID:
C3889329
Finding
HEMOGLOBIN FREIBURG
MedGen UID:
855029
Concept ID:
C3889330
Finding
HEMOGLOBIN FUKUOKA
MedGen UID:
855030
Concept ID:
C3889331
Finding
HEMOGLOBIN FUKUYAMA
MedGen UID:
855031
Concept ID:
C3889332
Finding
HEMOGLOBIN G (COPENHAGEN)
MedGen UID:
855032
Concept ID:
C3889333
Finding
HEMOGLOBIN G (COUSHATTA)
MedGen UID:
855033
Concept ID:
C3889334
Finding
HEMOGLOBIN G (FERRARA)
MedGen UID:
855034
Concept ID:
C3889335
Finding
HEMOGLOBIN G (GALVESTON)
MedGen UID:
855035
Concept ID:
C3889336
Finding
HEMOGLOBIN G (HSI-TSOU)
MedGen UID:
855036
Concept ID:
C3889337
Finding
HEMOGLOBIN G (MAKASSAR)
MedGen UID:
855037
Concept ID:
C3889338
Finding
HEMOGLOBIN G (SAN JOSE)
MedGen UID:
855038
Concept ID:
C3889339
Finding
HEMOGLOBIN G (SZUHU)
MedGen UID:
855039
Concept ID:
C3889340
Finding
HEMOGLOBIN G (TAIPEI)
MedGen UID:
855040
Concept ID:
C3889341
Finding
HEMOGLOBIN G (TAIWAN-AMI)
MedGen UID:
855041
Concept ID:
C3889342
Finding
HEMOGLOBIN GAINESVILLE-GA
MedGen UID:
855042
Concept ID:
C3889343
Finding
HEMOGLOBIN GAVELLO
MedGen UID:
855043
Concept ID:
C3889344
Finding
HEMOGLOBIN GEELONG
MedGen UID:
855044
Concept ID:
C3889345
Finding
HEMOGLOBIN GENOVA
MedGen UID:
855045
Concept ID:
C3889346
Finding
HEMOGLOBIN GRANGE-BLANCHE
MedGen UID:
855046
Concept ID:
C3889347
Finding
HEMOGLOBIN GUN HILL
MedGen UID:
855047
Concept ID:
C3889348
Finding
HEMOGLOBIN HAFNIA
MedGen UID:
855048
Concept ID:
C3889349
Finding
HEMOGLOBIN HAMADAN
MedGen UID:
855049
Concept ID:
C3889350
Finding
HEMOGLOBIN HAMILTON
MedGen UID:
855050
Concept ID:
C3889351
Finding
HEMOGLOBIN HAMMERSMITH
MedGen UID:
855051
Concept ID:
C3889352
Finding
HEMOGLOBIN HAZEBROUCK
MedGen UID:
855052
Concept ID:
C3889353
Finding
HEMOGLOBIN HEATHROW
MedGen UID:
855053
Concept ID:
C3889354
Finding
HEMOGLOBIN WACO
MedGen UID:
855058
Concept ID:
C3889359
Finding
HEMOGLOBIN GREAT LAKES
MedGen UID:
855059
Concept ID:
C3889360
Finding
HEMOGLOBIN BUENOS AIRES
MedGen UID:
855060
Concept ID:
C3889361
Finding
HEMOGLOBIN TOKUCHI
MedGen UID:
855061
Concept ID:
C3889362
Finding
HEMOGLOBIN D (LOS ANGELES)
MedGen UID:
855062
Concept ID:
C3889363
Finding
HEMOGLOBIN OAK RIDGE
MedGen UID:
855063
Concept ID:
C3889364
Finding
HEMOGLOBIN TOULOUSE
MedGen UID:
855064
Concept ID:
C3889365
Finding
HEMOGLOBIN J (COSENZA)
MedGen UID:
855065
Concept ID:
C3889366
Finding
HEMOGLOBIN MEILAHTI
MedGen UID:
855066
Concept ID:
C3889367
Finding
HEMOGLOBIN BUCURESTI
MedGen UID:
855067
Concept ID:
C3889368
Finding
HEMOGLOBIN LONG ISLAND
MedGen UID:
855068
Concept ID:
C3889369
Finding
HEMOGLOBIN NANCY
MedGen UID:
855069
Concept ID:
C3889370
Finding
HEMOGLOBIN FORT GORDON
MedGen UID:
855070
Concept ID:
C3889371
Finding
HEMOGLOBIN WARSAW
MedGen UID:
855071
Concept ID:
C3889372
Finding
HEMOGLOBIN LESLIE
MedGen UID:
855072
Concept ID:
C3889373
Finding
HEMOGLOBIN DEACONESS
MedGen UID:
855073
Concept ID:
C3889374
Finding
HEMOGLOBIN CASPER
MedGen UID:
855074
Concept ID:
C3889375
Finding
HEMOGLOBIN PETERBOROUGH
MedGen UID:
855328
Concept ID:
C3889844
Finding
HEMOGLOBIN PHILLY
MedGen UID:
855329
Concept ID:
C3889845
Finding
HEMOGLOBIN PIERRE-BENITE
MedGen UID:
855330
Concept ID:
C3889846
Finding
HEMOGLOBIN PITIE-SALPETRIERE
MedGen UID:
855331
Concept ID:
C3889847
Finding
HEMOGLOBIN POISSY
MedGen UID:
855333
Concept ID:
C3889849
Finding
HEMOGLOBIN PORTO ALEGRE
MedGen UID:
855334
Concept ID:
C3889850
Finding
HEMOGLOBIN POTOMAC
MedGen UID:
855335
Concept ID:
C3889851
Finding
HEMOGLOBIN PRESBYTERIAN
MedGen UID:
855337
Concept ID:
C3889853
Finding
HEMOGLOBIN PROVIDENCE
MedGen UID:
855338
Concept ID:
C3889854
Finding
HEMOGLOBIN PYRGOS
MedGen UID:
855339
Concept ID:
C3889855
Finding
HEMOGLOBIN QUIN-HAI
MedGen UID:
855340
Concept ID:
C3889856
Finding
HEMOGLOBIN RADCLIFFE
MedGen UID:
855342
Concept ID:
C3889858
Finding
HEMOGLOBIN RAHERE
MedGen UID:
855343
Concept ID:
C3889859
Finding
HEMOGLOBIN RAINIER
MedGen UID:
855344
Concept ID:
C3889860
Finding
HEMOGLOBIN RALEIGH
MedGen UID:
855345
Concept ID:
C3889861
Finding
HEMOGLOBIN RANDWICK
MedGen UID:
855347
Concept ID:
C3889863
Finding
HEMOGLOBIN REGINA
MedGen UID:
855348
Concept ID:
C3889864
Finding
HEMOGLOBIN RICHMOND
MedGen UID:
855349
Concept ID:
C3889865
Finding
HEMOGLOBIN RIO GRANDE
MedGen UID:
855350
Concept ID:
C3889866
Finding
HEMOGLOBIN RIVERDALE-BRONX
MedGen UID:
855351
Concept ID:
C3889867
Finding
HEMOGLOBIN RIYADH
MedGen UID:
855352
Concept ID:
C3889868
Finding
HEMOGLOBIN ROSEAU-POINTE A PITRE
MedGen UID:
855353
Concept ID:
C3889869
Finding
HEMOGLOBIN ROTHSCHILD
MedGen UID:
855354
Concept ID:
C3889870
Finding
HEMOGLOBIN RUSH
MedGen UID:
855355
Concept ID:
C3889871
Finding
HEMOGLOBIN SABINE
MedGen UID:
855356
Concept ID:
C3889872
Finding
HEMOGLOBIN SAINT ETIENNE
MedGen UID:
855357
Concept ID:
C3889873
Finding
HEMOGLOBIN SAINT JACQUES
MedGen UID:
855358
Concept ID:
C3889874
Finding
HEMOGLOBIN SAITAMA
MedGen UID:
855359
Concept ID:
C3889875
Finding
HEMOGLOBIN SAKI
MedGen UID:
855360
Concept ID:
C3889876
Finding
HEMOGLOBIN SAN DIEGO
MedGen UID:
855362
Concept ID:
C3889878
Finding
HEMOGLOBIN SANTA ANA
MedGen UID:
855363
Concept ID:
C3889879
Finding
HEMOGLOBIN SAVANNAH
MedGen UID:
855364
Concept ID:
C3889880
Finding
HEMOGLOBIN SAVERNE
MedGen UID:
855365
Concept ID:
C3889881
Finding
HEMOGLOBIN SOUTH FLORIDA
MedGen UID:
855367
Concept ID:
C3889883
Finding
HEMOGLOBIN SOUTHAMPTON
MedGen UID:
855368
Concept ID:
C3889884
Finding
HEMOGLOBIN ST. ANTOINE
MedGen UID:
855370
Concept ID:
C3889886
Finding
HEMOGLOBIN ST. LOUIS
MedGen UID:
855371
Concept ID:
C3889887
Finding
HEMOGLOBIN ST. MANDE
MedGen UID:
855372
Concept ID:
C3889888
Finding
HEMOGLOBIN STANMORE
MedGen UID:
855373
Concept ID:
C3889889
Finding
HEMOGLOBIN STRASBOURG
MedGen UID:
855374
Concept ID:
C3889890
Finding
HEMOGLOBIN BRUXELLES
MedGen UID:
855377
Concept ID:
C3889893
Finding
HEMOGLOBIN BRYN MAWR
MedGen UID:
855378
Concept ID:
C3889894
Finding
HEMOGLOBIN BUNBURY
MedGen UID:
855379
Concept ID:
C3889895
Finding
HEMOGLOBIN BURKE
MedGen UID:
855380
Concept ID:
C3889896
Finding
HEMOGLOBIN BUSHWICK
MedGen UID:
855381
Concept ID:
C3889897
Finding
HEMOGLOBIN C
MedGen UID:
855382
Concept ID:
C3889898
Finding
HEMOGLOBIN CAMDEN
MedGen UID:
855383
Concept ID:
C3889899
Finding
HEMOGLOBIN CAMPERDOWN
MedGen UID:
855384
Concept ID:
C3889900
Finding
HEMOGLOBIN CARIBBEAN
MedGen UID:
855386
Concept ID:
C3889902
Finding
HEMOGLOBIN CASTILLA
MedGen UID:
855387
Concept ID:
C3889903
Finding
HEMOGLOBIN CHANDIGARH
MedGen UID:
855388
Concept ID:
C3889904
Finding
HEMOGLOBIN CHEMILLY
MedGen UID:
855390
Concept ID:
C3889906
Finding
HEMOGLOBIN CHEVERLY
MedGen UID:
855391
Concept ID:
C3889907
Finding
HEMOGLOBIN CHICO
MedGen UID:
855392
Concept ID:
C3889908
Finding
HEMOGLOBIN CHRISTCHURCH
MedGen UID:
855393
Concept ID:
C3889909
Finding
HEMOGLOBIN CITY OF HOPE
MedGen UID:
855394
Concept ID:
C3889910
Finding
HEMOGLOBIN COCHIN-PORT ROYAL
MedGen UID:
855396
Concept ID:
C3889912
Finding
HEMOGLOBIN COCODY
MedGen UID:
855397
Concept ID:
C3889913
Finding
HEMOGLOBIN HELSINKI
MedGen UID:
855398
Concept ID:
C3889914
Finding
HEMOGLOBIN HENRI MONDOR
MedGen UID:
855399
Concept ID:
C3889915
Finding
HEMOGLOBIN HIJIYAMA
MedGen UID:
855400
Concept ID:
C3889916
Finding
HEMOGLOBIN HIKARI
MedGen UID:
855401
Concept ID:
C3889917
Finding
HEMOGLOBIN HIMEJI
MedGen UID:
855402
Concept ID:
C3889918
Finding
HEMOGLOBIN HINSDALE
MedGen UID:
855403
Concept ID:
C3889919
Finding
HEMOGLOBIN HIROSE
MedGen UID:
855404
Concept ID:
C3889920
Finding
HEMOGLOBIN HIROSHIMA
MedGen UID:
855405
Concept ID:
C3889921
Finding
HEMOGLOBIN HOFU
MedGen UID:
855406
Concept ID:
C3889922
Finding
HEMOGLOBIN HOPE
MedGen UID:
855407
Concept ID:
C3889923
Finding
HEMOGLOBIN HOSHIDA
MedGen UID:
855408
Concept ID:
C3889924
Finding
HEMOGLOBIN HOTEL-DIEU
MedGen UID:
855409
Concept ID:
C3889925
Finding
HEMOGLOBIN I (HIGH WYCOMBE)
MedGen UID:
855410
Concept ID:
C3889926
Finding
HEMOGLOBIN I (TOULOUSE)
MedGen UID:
855411
Concept ID:
C3889927
Finding
HEMOGLOBIN INDIANAPOLIS
MedGen UID:
855412
Concept ID:
C3889928
Finding
HEMOGLOBIN J (ALTGELD GARDENS)
MedGen UID:
855413
Concept ID:
C3889929
Finding
HEMOGLOBIN J (AMIENS)
MedGen UID:
855414
Concept ID:
C3889930
Finding
HEMOGLOBIN J (ANTAKYA)
MedGen UID:
855415
Concept ID:
C3889931
Finding
HEMOGLOBIN J (AUCKLAND)
MedGen UID:
855416
Concept ID:
C3889932
Finding
HEMOGLOBIN J (BALTIMORE)
MedGen UID:
855417
Concept ID:
C3889933
Finding
HEMOGLOBIN J (BANGKOK)
MedGen UID:
855418
Concept ID:
C3889934
Finding
HEMOGLOBIN J (CAIRO)
MedGen UID:
855419
Concept ID:
C3889935
Finding
HEMOGLOBIN J (CALABRIA)
MedGen UID:
855420
Concept ID:
C3889936
Finding
HEMOGLOBIN J (CHICAGO)
MedGen UID:
855421
Concept ID:
C3889937
Finding
HEMOGLOBIN J (DALOA)
MedGen UID:
855422
Concept ID:
C3889938
Finding
HEMOGLOBIN J (GUANTANAMO)
MedGen UID:
855423
Concept ID:
C3889939
Finding
HEMOGLOBIN J (IRAN)
MedGen UID:
855424
Concept ID:
C3889940
Finding
HEMOGLOBIN J (LENS)
MedGen UID:
855425
Concept ID:
C3889941
Finding
HEMOGLOBIN J (LOME)
MedGen UID:
855426
Concept ID:
C3889942
Finding
HEMOGLOBIN J (LUHE)
MedGen UID:
855427
Concept ID:
C3889943
Finding
HEMOGLOBIN J (SICILIA)
MedGen UID:
855428
Concept ID:
C3889944
Finding
HEMOGLOBIN J (TAICHUNG)
MedGen UID:
855429
Concept ID:
C3889945
Finding
HEMOGLOBIN JIANGHUA
MedGen UID:
855430
Concept ID:
C3889946
Finding
HEMOGLOBIN JOHNSTOWN
MedGen UID:
855431
Concept ID:
C3889947
Finding
HEMOGLOBIN K (CAMEROON)
MedGen UID:
855432
Concept ID:
C3889948
Finding
HEMOGLOBIN K (IBADAN)
MedGen UID:
855433
Concept ID:
C3889949
Finding
HEMOGLOBIN K (WOOLWICH)
MedGen UID:
855434
Concept ID:
C3889950
Finding
HEMOGLOBIN KANSAS
MedGen UID:
855435
Concept ID:
C3889951
Finding
HEMOGLOBIN KEMPSEY
MedGen UID:
855436
Concept ID:
C3889952
Finding
HEMOGLOBIN KENITRA
MedGen UID:
855437
Concept ID:
C3889953
Finding
HEMOGLOBIN KHARTOUM
MedGen UID:
855438
Concept ID:
C3889954
Finding
HEMOGLOBIN KNOSSOS
MedGen UID:
855439
Concept ID:
C3889955
Finding
HEMOGLOBIN KOFU
MedGen UID:
855440
Concept ID:
C3889956
Finding
HEMOGLOBIN KOLN
MedGen UID:
855441
Concept ID:
C3889957
Finding
HEMOGLOBIN KORIYAMA
MedGen UID:
855442
Concept ID:
C3889958
Finding
HEMOGLOBIN KORLE-BU
MedGen UID:
855443
Concept ID:
C3889959
Finding
HEMOGLOBIN LA DESIRADE
MedGen UID:
855444
Concept ID:
C3889960
Finding
HEMOGLOBIN HACETTEPE
MedGen UID:
855446
Concept ID:
C3889962
Finding
HEMOGLOBIN DHOFAR
MedGen UID:
855451
Concept ID:
C3889967
Finding
HEMOGLOBIN GENEVA
MedGen UID:
855452
Concept ID:
C3889968
Finding
HEMOGLOBIN SENDAGI
MedGen UID:
855586
Concept ID:
C3890358
Finding
HEMOGLOBIN SHANGHAI
MedGen UID:
855587
Concept ID:
C3890359
Finding
HEMOGLOBIN SEATTLE
MedGen UID:
855588
Concept ID:
C3890360
Finding
HEMOGLOBIN SHELBY
MedGen UID:
855589
Concept ID:
C3890361
Finding
HEMOGLOBIN SHEPHERDS BUSH
MedGen UID:
855590
Concept ID:
C3890363
Finding
HEMOGLOBIN SHERWOOD FOREST
MedGen UID:
855591
Concept ID:
C3890364
Finding
HEMOGLOBIN SHOWA-YAKUSHIJI
MedGen UID:
855592
Concept ID:
C3890366
Finding
HEMOGLOBIN SIRIRAJ
MedGen UID:
855593
Concept ID:
C3890368
Finding
HEMOGLOBIN SOGN
MedGen UID:
855594
Concept ID:
C3890369
Finding
HEMOGLOBIN YPSILANTI
MedGen UID:
855640
Concept ID:
C3890416
Finding
HEMOGLOBIN YUSA
MedGen UID:
855641
Concept ID:
C3890417
Finding
HEMOGLOBIN ZURICH
MedGen UID:
855642
Concept ID:
C3890418
Finding
HEMOGLOBIN LAS PALMAS
MedGen UID:
855759
Concept ID:
C3890755
Finding
HEMOGLOBIN LEIDEN
MedGen UID:
855760
Concept ID:
C3890756
Finding
HEMOGLOBIN LINCOLN PARK
MedGen UID:
855761
Concept ID:
C3890757
Finding
HEMOGLOBIN LINKOPING
MedGen UID:
855762
Concept ID:
C3890758
Finding
HEMOGLOBIN LITTLE ROCK
MedGen UID:
855763
Concept ID:
C3890759
Finding
HEMOGLOBIN LOUISVILLE
MedGen UID:
855764
Concept ID:
C3890760
Finding
HEMOGLOBIN LUFKIN
MedGen UID:
855765
Concept ID:
C3890761
Finding
HEMOGLOBIN LYON
MedGen UID:
855766
Concept ID:
C3890762
Finding
HEMOGLOBIN MACHIDA
MedGen UID:
855767
Concept ID:
C3890763
Finding
HEMOGLOBIN MADRID
MedGen UID:
855768
Concept ID:
C3890764
Finding
HEMOGLOBIN MALAY
MedGen UID:
855769
Concept ID:
C3890765
Finding
HEMOGLOBIN MALMO
MedGen UID:
855770
Concept ID:
C3890766
Finding
HEMOGLOBIN MAPUTO
MedGen UID:
855772
Concept ID:
C3890768
Finding
HEMOGLOBIN MARSEILLE
MedGen UID:
855773
Concept ID:
C3890769
Finding
HEMOGLOBIN MASUDA
MedGen UID:
855774
Concept ID:
C3890770
Finding
HEMOGLOBIN MATERA
MedGen UID:
855775
Concept ID:
C3890771
Finding
HEMOGLOBIN M (SASKATOON)
MedGen UID:
855906
Concept ID:
C3891120
Finding
HEMOGLOBIN MEQUON
MedGen UID:
855907
Concept ID:
C3891121
Finding
HEMOGLOBIN MCKEES ROCKS
MedGen UID:
855908
Concept ID:
C3891122
Finding
HEMOGLOBIN MINNEAPOLIS-LAOS
MedGen UID:
855909
Concept ID:
C3891123
Finding
HEMOGLOBIN MISSISSIPPI
MedGen UID:
855910
Concept ID:
C3891124
Finding
HEMOGLOBIN MITO
MedGen UID:
855911
Concept ID:
C3891125
Finding
HEMOGLOBIN MIYADA
MedGen UID:
855912
Concept ID:
C3891126
Finding
HEMOGLOBIN MIYASHIRO
MedGen UID:
855913
Concept ID:
C3891127
Finding
HEMOGLOBIN MIZUHO
MedGen UID:
855914
Concept ID:
C3891128
Finding
HEMOGLOBIN MOBILE
MedGen UID:
855915
Concept ID:
C3891129
Finding
HEMOGLOBIN MORIGUCHI
MedGen UID:
855916
Concept ID:
C3891130
Finding
HEMOGLOBIN MOSCVA
MedGen UID:
855917
Concept ID:
C3891131
Finding
HEMOGLOBIN MOZHAISK
MedGen UID:
855918
Concept ID:
C3891132
Finding
HEMOGLOBIN N (BALTIMORE)
MedGen UID:
855919
Concept ID:
C3891133
Finding
HEMOGLOBIN N (SEATTLE)
MedGen UID:
855920
Concept ID:
C3891134
Finding
HEMOGLOBIN NAGASAKI
MedGen UID:
855921
Concept ID:
C3891135
Finding
HEMOGLOBIN NAGOYA
MedGen UID:
855922
Concept ID:
C3891136
Finding
HEMOGLOBIN NEVERS
MedGen UID:
855923
Concept ID:
C3891137
Finding
HEMOGLOBIN NEW MEXICO
MedGen UID:
855924
Concept ID:
C3891138
Finding
HEMOGLOBIN NEW YORK
MedGen UID:
855925
Concept ID:
C3891139
Finding
HEMOGLOBIN NEWCASTLE
MedGen UID:
855926
Concept ID:
C3891140
Finding
HEMOGLOBIN NITEROI
MedGen UID:
855927
Concept ID:
C3891141
Finding
HEMOGLOBIN NORTH CHICAGO
MedGen UID:
855928
Concept ID:
C3891142
Finding
HEMOGLOBIN NORTH SHORE
MedGen UID:
855929
Concept ID:
C3891143
Finding
HEMOGLOBIN NOTTINGHAM
MedGen UID:
855930
Concept ID:
C3891144
Finding
HEMOGLOBIN O (ARAB)
MedGen UID:
855931
Concept ID:
C3891145
Finding
HEMOGLOBIN OCHO RIOS
MedGen UID:
855932
Concept ID:
C3891146
Finding
HEMOGLOBIN OHIO
MedGen UID:
855933
Concept ID:
C3891147
Finding
HEMOGLOBIN OKALOOSA
MedGen UID:
855934
Concept ID:
C3891148
Finding
HEMOGLOBIN OKAYAMA
MedGen UID:
855935
Concept ID:
C3891149
Finding
HEMOGLOBIN OKAZAKI
MedGen UID:
855936
Concept ID:
C3891150
Finding
HEMOGLOBIN COLLINGWOOD
MedGen UID:
855937
Concept ID:
C3891151
Finding
HEMOGLOBIN MONROE
MedGen UID:
855938
Concept ID:
C3891152
Finding
HEMOGLOBIN AALBORG
MedGen UID:
855969
Concept ID:
C3891407
Finding
HEMOGLOBIN ABRUZZO
MedGen UID:
855970
Concept ID:
C3891408
Finding
HEMOGLOBIN AGENOGI
MedGen UID:
855971
Concept ID:
C3891409
Finding
HEMOGLOBIN ALABAMA
MedGen UID:
855974
Concept ID:
C3891412
Finding
HEMOGLOBIN ALAMO
MedGen UID:
855975
Concept ID:
C3891413
Finding
HEMOGLOBIN ALBERTA
MedGen UID:
855977
Concept ID:
C3891415
Finding
HEMOGLOBIN ALTDORF
MedGen UID:
855997
Concept ID:
C3891435
Finding
HEMOGLOBIN ANDREW-MINNEAPOLIS
MedGen UID:
855998
Concept ID:
C3891436
Finding
HEMOGLOBIN OLMSTED
MedGen UID:
855999
Concept ID:
C3891437
Finding
HEMOGLOBIN OLOMOUC
MedGen UID:
856000
Concept ID:
C3891438
Finding
HEMOGLOBIN OLYMPIA
MedGen UID:
856001
Concept ID:
C3891439
Finding
HEMOGLOBIN OSLER
MedGen UID:
856002
Concept ID:
C3891440
Finding
HEMOGLOBIN OSU CHRISTIANSBORG
MedGen UID:
856003
Concept ID:
C3891441
Finding
HEMOGLOBIN P
MedGen UID:
856004
Concept ID:
C3891442
Finding
HEMOGLOBIN P (CONGO)
MedGen UID:
856005
Concept ID:
C3891443
Finding
HEMOGLOBIN P (NILOTIC)
MedGen UID:
856006
Concept ID:
C3891444
Finding
HEMOGLOBIN PALMERSTON NORTH
MedGen UID:
856007
Concept ID:
C3891445
Finding
HEMOGLOBIN S (ANTILLES)
MedGen UID:
856008
Concept ID:
C3891446
Finding
HEMOGLOBIN S (TRAVIS)
MedGen UID:
856009
Concept ID:
C3891447
Finding
HEMOGLOBIN ANKARA
MedGen UID:
856034
Concept ID:
C3891665
Finding
HEMOGLOBIN ARLINGTON PARK
MedGen UID:
856035
Concept ID:
C3891666
Finding
HEMOGLOBIN ATHENS-GEORGIA
MedGen UID:
856036
Concept ID:
C3891667
Finding
HEMOGLOBIN ATLANTA
MedGen UID:
856037
Concept ID:
C3891668
Finding
HEMOGLOBIN ATLANTA-COVENTRY
MedGen UID:
856038
Concept ID:
C3891669
Finding
HEMOGLOBIN AUSTIN
MedGen UID:
856039
Concept ID:
C3891670
Finding
HEMOGLOBIN AVICENNA
MedGen UID:
856040
Concept ID:
C3891671
Finding
HEMOGLOBIN BARCELONA
MedGen UID:
856041
Concept ID:
C3891672
Finding
HEMOGLOBIN BAYLOR
MedGen UID:
856042
Concept ID:
C3891673
Finding
HEMOGLOBIN BEIRUT
MedGen UID:
856043
Concept ID:
C3891674
Finding
HEMOGLOBIN BELFAST
MedGen UID:
856044
Concept ID:
C3891675
Finding
HEMOGLOBIN C (GEORGETOWN)
MedGen UID:
856045
Concept ID:
C3891676
Finding
HEMOGLOBIN C (ZIGUINCHOR)
MedGen UID:
856046
Concept ID:
C3891677
Finding
HEMOGLOBIN CONNECTICUT
MedGen UID:
856047
Concept ID:
C3891678
Finding
HEMOGLOBIN COVENTRY
MedGen UID:
856048
Concept ID:
C3891679
Finding
HEMOGLOBIN SUMMER HILL
MedGen UID:
856049
Concept ID:
C3891680
Finding
HEMOGLOBIN SUNNYBROOK
MedGen UID:
856050
Concept ID:
C3891681
Finding
HEMOGLOBIN SYDNEY
MedGen UID:
856051
Concept ID:
C3891682
Finding
HEMOGLOBIN SYRACUSE
MedGen UID:
856052
Concept ID:
C3891683
Finding
HEMOGLOBIN T (CAMBODIA)
MedGen UID:
856053
Concept ID:
C3891684
Finding
HEMOGLOBIN TA-LI
MedGen UID:
856054
Concept ID:
C3891685
Finding
HEMOGLOBIN TACOMA
MedGen UID:
856055
Concept ID:
C3891686
Finding
HEMOGLOBIN TAK
MedGen UID:
856056
Concept ID:
C3891687
Finding
HEMOGLOBIN TAKAMATSU
MedGen UID:
856057
Concept ID:
C3891688
Finding
HEMOGLOBIN TAMPA
MedGen UID:
856058
Concept ID:
C3891689
Finding
HEMOGLOBIN TIANSHUI
MedGen UID:
856059
Concept ID:
C3891690
Finding
HEMOGLOBIN TOCHIGI
MedGen UID:
856060
Concept ID:
C3891691
Finding
HEMOGLOBIN TOURS
MedGen UID:
856061
Concept ID:
C3891692
Finding
HEMOGLOBIN TOYOAKE
MedGen UID:
856062
Concept ID:
C3891693
Finding
HEMOGLOBIN TUBINGEN
MedGen UID:
856063
Concept ID:
C3891694
Finding
HEMOGLOBIN TUNIS
MedGen UID:
856064
Concept ID:
C3891695
Finding
HEMOGLOBIN TY GARD
MedGen UID:
856065
Concept ID:
C3891696
Finding
HEMOGLOBIN VAASA
MedGen UID:
856066
Concept ID:
C3891697
Finding
HEMOGLOBIN VANCOUVER
MedGen UID:
856067
Concept ID:
C3891698
Finding
HEMOGLOBIN VANDERBILT
MedGen UID:
856068
Concept ID:
C3891699
Finding
HEMOGLOBIN VICKSBURG
MedGen UID:
856069
Concept ID:
C3891700
Finding
HEMOGLOBIN VILLEJUIF
MedGen UID:
856070
Concept ID:
C3891701
Finding
HEMOGLOBIN VOLGA
MedGen UID:
856071
Concept ID:
C3891702
Finding
HEMOGLOBIN WARWICKSHIRE
MedGen UID:
856072
Concept ID:
C3891703
Finding
HEMOGLOBIN WIEN
MedGen UID:
856073
Concept ID:
C3891704
Finding
HEMOGLOBIN WILLAMETTE
MedGen UID:
856074
Concept ID:
C3891705
Finding
HEMOGLOBIN WINDSOR
MedGen UID:
856075
Concept ID:
C3891706
Finding
HEMOGLOBIN WOOD
MedGen UID:
856076
Concept ID:
C3891707
Finding
HEMOGLOBIN YAKIMA
MedGen UID:
856077
Concept ID:
C3891708
Finding
HEMOGLOBIN YAMAGATA
MedGen UID:
856078
Concept ID:
C3891709
Finding
HEMOGLOBIN YATSUSHIRO
MedGen UID:
856079
Concept ID:
C3891710
Finding
HEMOGLOBIN YOKOHAMA
MedGen UID:
856080
Concept ID:
C3891711
Finding
HEMOGLOBIN YORK
MedGen UID:
856081
Concept ID:
C3891712
Finding
HEMOGLOBIN YOSHIZUKA
MedGen UID:
856097
Concept ID:
C3891918
Finding
HEMOGLOBIN P (GALVESTON)
MedGen UID:
856156
Concept ID:
C3892932
Finding
HEMOGLOBIN M (HYDE PARK)
MedGen UID:
856158
Concept ID:
C3892934
Finding
HEMOGLOBIN MS
MedGen UID:
856159
Concept ID:
C3892935
Finding
HEMOGLOBIN C (HARLEM)
MedGen UID:
856162
Concept ID:
C3893182
Finding
Immunodeficiency 27b
MedGen UID:
863300
Concept ID:
C4014863
Disease or Syndrome
Immunodeficiency-27B results from autosomal dominant (AD) IFNGR1 deficiency. Patients with AD IFNGR1 deficiency commonly present with recurrent, moderately severe infections with environmental mycobacteria or bacillus Calmette-Guerin (BCG). In contrast with patients with complete autosomal recessive (AR) IFNGR1 deficiency (IMD27A), cells from patients with AD IFNGR1 deficiency display residual responses to IFNG in vitro, indicating that the deficiency in IFNGR1 is partial. The clinical features of AD IFNGR1 deficiency are usually less severe than those in children with complete AR IFNGR1 deficiency, and mycobacterial infection often occurs later (mean age of 13.4 years vs 1.3 years), with patients having longer mean disease-free survival. In patients with AD IFNGR1 deficiency, M. avium tends to cause unifocal or multifocal osteomyelitis. Salmonellosis is present in about 5% of patients with AR or AD IFNGR1 deficiency, and other infections have been reported in single patients (review by Al-Muhsen and Casanova, 2008).
HEMOGLOBIN G (ACCRA)
MedGen UID:
864596
Concept ID:
C4016159
Finding
HEMOGLOBIN ISTANBUL
MedGen UID:
864597
Concept ID:
C4016160
Finding
HEMOGLOBIN J (CORDOBA)
MedGen UID:
864598
Concept ID:
C4016161
Finding
HEMOGLOBIN J (KAOHSIUNG)
MedGen UID:
864599
Concept ID:
C4016162
Finding
HEMOGLOBIN J (RAMBAM)
MedGen UID:
864600
Concept ID:
C4016163
Finding
HEMOGLOBIN KAIROUAN
MedGen UID:
864601
Concept ID:
C4016164
Finding
HEMOGLOBIN M (MILWAUKEE 1)
MedGen UID:
864602
Concept ID:
C4016165
Finding
HEMOGLOBIN M (MILWAUKEE 2)
MedGen UID:
864603
Concept ID:
C4016166
Finding
HEMOGLOBIN MIZUNAMI
MedGen UID:
864604
Concept ID:
C4016167
Finding
HEMOGLOBIN N, BETA TYPE
MedGen UID:
864605
Concept ID:
C4016168
Finding
HEMOGLOBIN N (MEMPHIS)
MedGen UID:
864606
Concept ID:
C4016169
Finding
HEMOGLOBIN N (TIMONE)
MedGen UID:
864607
Concept ID:
C4016170
Finding
HEMOGLOBIN S (OMAN)
MedGen UID:
864608
Concept ID:
C4016171
Finding
HEMOGLOBIN S (PROVIDENCE)
MedGen UID:
864609
Concept ID:
C4016172
Finding
HEMOGLOBIN TILBURG
MedGen UID:
864610
Concept ID:
C4016173
Finding
HEMOGLOBIN YUKUHASHI
MedGen UID:
864611
Concept ID:
C4016174
Finding
HEMOGLOBIN HOUSTON
MedGen UID:
864612
Concept ID:
C4016175
Finding
HEMOGLOBIN D (CAMPERDOWN)
MedGen UID:
865901
Concept ID:
C4017464
Finding
HEINZ BODY HEMOLYTIC ANEMIA
MedGen UID:
865902
Concept ID:
C4017465
Disease or Syndrome
HEMOGLOBIN ZIGUINCHOR
MedGen UID:
865903
Concept ID:
C4017466
Finding
HEMOGLOBIN MOTOWN
MedGen UID:
865904
Concept ID:
C4017467
Finding
HEMOGLOBIN D (CHICAGO)
MedGen UID:
865905
Concept ID:
C4017468
Finding
HEMOGLOBIN D (NORTH CAROLINA)
MedGen UID:
865906
Concept ID:
C4017469
Finding
HEMOGLOBIN D (PORTUGAL)
MedGen UID:
865907
Concept ID:
C4017470
Finding
BETA-E-THALASSEMIA
MedGen UID:
865908
Concept ID:
C4017471
Finding
HEMOGLOBIN M (FREIBURG)
MedGen UID:
865909
Concept ID:
C4017472
Finding
HEMOGLOBIN G (SASKATOON)
MedGen UID:
865910
Concept ID:
C4017473
Finding
HEMOGLOBIN G (HSIN-CHU)
MedGen UID:
865911
Concept ID:
C4017474
Finding
HEMOGLOBIN G (TAEGU)
MedGen UID:
865912
Concept ID:
C4017475
Finding
HEMOGLOBIN G (PORT ARTHUR)
MedGen UID:
865913
Concept ID:
C4017476
Finding
HEMOGLOBIN G (TEXAS)
MedGen UID:
865914
Concept ID:
C4017477
Finding
HEMOGLOBIN GIFU
MedGen UID:
865915
Concept ID:
C4017478
Finding
HEMOGLOBIN JINAN
MedGen UID:
865916
Concept ID:
C4017479
Finding
HEMOGLOBIN HYOGO
MedGen UID:
865917
Concept ID:
C4017480
Finding
HEMOGLOBIN CHIBA
MedGen UID:
865918
Concept ID:
C4017481
Finding
HEMOGLOBIN CHAYA
MedGen UID:
865919
Concept ID:
C4017482
Finding
HEMOGLOBIN J (IRELAND)
MedGen UID:
865920
Concept ID:
C4017483
Finding
HEMOGLOBIN J (TRINIDAD)
MedGen UID:
865921
Concept ID:
C4017484
Finding
HEMOGLOBIN J (GEORGIA)
MedGen UID:
865922
Concept ID:
C4017485
Finding
HEMOGLOBIN N (NEW HAVEN 2)
MedGen UID:
865923
Concept ID:
C4017486
Finding
HEMOGLOBIN J (KORAT)
MedGen UID:
865924
Concept ID:
C4017487
Finding
HEMOGLOBIN J (MANADO)
MedGen UID:
865925
Concept ID:
C4017488
Finding
HEMOGLOBIN J (MEINUNG)
MedGen UID:
865926
Concept ID:
C4017489
Finding
HEMOGLOBIN J (BARI)
MedGen UID:
865927
Concept ID:
C4017490
Finding
HEMOGLOBIN J (HONOLULU)
MedGen UID:
865928
Concept ID:
C4017491
Finding
HEMOGLOBIN J (CAMBRIDGE)
MedGen UID:
865929
Concept ID:
C4017492
Finding
HEMOGLOBIN REISSMANN ET AL.
MedGen UID:
865930
Concept ID:
C4017493
Finding
Beta-knossos-thalassemia
MedGen UID:
865931
Concept ID:
C4017494
Finding
HEMOGLOBIN UBE-1
MedGen UID:
865932
Concept ID:
C4017495
Finding
HEMOGLOBIN SAN FRANCISCO (PACIFIC)
MedGen UID:
865933
Concept ID:
C4017496
Finding
HBB/HBD ANTI-LEPORE
MedGen UID:
865934
Concept ID:
C4017497
Finding
HEMOGLOBIN M (AKITA)
MedGen UID:
865935
Concept ID:
C4017498
Finding
HEMOGLOBIN M (ARHUS)
MedGen UID:
865936
Concept ID:
C4017499
Finding
HEMOGLOBIN M (CHICAGO)
MedGen UID:
865937
Concept ID:
C4017500
Finding
HEMOGLOBIN M (EMORY)
MedGen UID:
865938
Concept ID:
C4017501
Finding
HEMOGLOBIN M (ERLANGEN)
MedGen UID:
865939
Concept ID:
C4017502
Finding
HEMOGLOBIN M (HAMBURG)
MedGen UID:
865940
Concept ID:
C4017503
Finding
HEMOGLOBIN M (HIDA)
MedGen UID:
865941
Concept ID:
C4017504
Finding
HEMOGLOBIN M (HORLEIN-WEBER)
MedGen UID:
865942
Concept ID:
C4017505
Finding
HEMOGLOBIN M (KURUME)
MedGen UID:
865943
Concept ID:
C4017506
Finding
HEMOGLOBIN M (LEIPZIG)
MedGen UID:
865944
Concept ID:
C4017507
Finding
HEMOGLOBIN M (NOVI SAD)
MedGen UID:
865945
Concept ID:
C4017508
Finding
HEMOGLOBIN M (RADOM)
MedGen UID:
865946
Concept ID:
C4017509
Finding
Beta-malay-thalassemia
MedGen UID:
865947
Concept ID:
C4017510
Finding
HEMOGLOBIN N (JENKINS)
MedGen UID:
865948
Concept ID:
C4017511
Finding
HEMOGLOBIN JENKINS
MedGen UID:
865949
Concept ID:
C4017512
Finding
HEMOGLOBIN HOPKINS 1
MedGen UID:
865950
Concept ID:
C4017513
Finding
HEMOGLOBIN KENWOOD
MedGen UID:
865951
Concept ID:
C4017514
Finding
HEMOGLOBIN KAOHSIUNG
MedGen UID:
865952
Concept ID:
C4017515
Finding
HEMOGLOBIN NORTH SHORE-CARACAS
MedGen UID:
865953
Concept ID:
C4017516
Finding
HEMOGLOBIN EGYPT
MedGen UID:
865954
Concept ID:
C4017517
Finding
HEMOGLOBIN ABRAHAM LINCOLN
MedGen UID:
865955
Concept ID:
C4017518
Finding
HEMOGLOBIN KOBE
MedGen UID:
865956
Concept ID:
C4017519
Finding
HEMOGLOBIN KARATSU
MedGen UID:
865957
Concept ID:
C4017520
Finding
HEMOGLOBIN S/O (ARAB)
MedGen UID:
865958
Concept ID:
C4017521
Finding
Beta-showa-yakushiji thalassemia
MedGen UID:
865959
Concept ID:
C4017522
Finding
HEMOGLOBIN G (HONAN)
MedGen UID:
865960
Concept ID:
C4017523
Finding
HEMOGLOBIN DRENTHE
MedGen UID:
865961
Concept ID:
C4017524
Finding
Beta-plus-thalassemia, dominant
MedGen UID:
865962
Concept ID:
C4017525
Finding
BETA-HOUSTON-THALASSEMIA
MedGen UID:
865963
Concept ID:
C4017526
Finding
HEMOGLOBIN CAGLIARI
MedGen UID:
865964
Concept ID:
C4017527
Finding
Beta-thalassemia, lermontov type
MedGen UID:
865965
Concept ID:
C4017528
Finding
Dominant beta-thalassemia
MedGen UID:
897183
Concept ID:
C4274391
Disease or Syndrome
Dominant beta-thalassaemia is a form of beta-thalassaemia resulting in moderate to severe anaemia. Prevalence of this form is not known. Presents with moderate to severe anaemia, jaundice and splenomegaly. Rare mutations in the beta-globin HBB gene result in synthesis of extremely unstable beta-globin variants which precipitate in erythroid precursors causing ineffective erythropoiesis.
HEMOGLOBIN ISEHARA
MedGen UID:
924378
Concept ID:
C4283831
Finding
HEMOGLOBIN AURORA
MedGen UID:
924475
Concept ID:
C4283964
Finding
HEMOGLOBIN SPARTA
MedGen UID:
924476
Concept ID:
C4283965
Finding
HEMOGLOBIN SARREBOURG
MedGen UID:
924481
Concept ID:
C4283974
Finding
HEMOGLOBIN YAOUNDE
MedGen UID:
924486
Concept ID:
C4283981
Finding
HEMOGLOBIN CHESTERFIELD
MedGen UID:
924489
Concept ID:
C4283985
Finding
HEMOGLOBIN LUCKNOW
MedGen UID:
924490
Concept ID:
C4283986
Finding
HEMOGLOBIN BOLOGNA-ST. ORSOLA
MedGen UID:
924492
Concept ID:
C4283988
Finding
HEMOGLOBIN HIGASHITOCHIGI
MedGen UID:
924493
Concept ID:
C4283989
Finding
HEMOGLOBIN BIRMINGHAM
MedGen UID:
924499
Concept ID:
C4283995
Finding
HEMOGLOBIN MARINEO
MedGen UID:
924500
Concept ID:
C4283996
Finding
HEMOGLOBIN LIMASSOL
MedGen UID:
924501
Concept ID:
C4283997
Finding
HEMOGLOBIN MONTREAL
MedGen UID:
924502
Concept ID:
C4283998
Finding
HB AUBENAS
MedGen UID:
924544
Concept ID:
C4284047
Finding
HEMOGLOBIN BRESCIA
MedGen UID:
924546
Concept ID:
C4284049
Finding
HB GAMBARA
MedGen UID:
924547
Concept ID:
C4284050
Finding
HEMOGLOBIN NEAPOLIS
MedGen UID:
924552
Concept ID:
C4284055
Finding
HEMOGLOBIN MUSKEGON
MedGen UID:
924587
Concept ID:
C4284105
Finding
HEMOGLOBIN NAKANO
MedGen UID:
924588
Concept ID:
C4284106
Finding
HEMOGLOBIN NIJKERK
MedGen UID:
924591
Concept ID:
C4284109
Finding
HEMOGLOBIN NIKOSIA
MedGen UID:
924592
Concept ID:
C4284110
Finding
HEMOGLOBIN IOWA
MedGen UID:
924621
Concept ID:
C4284147
Finding
HEMOGLOBIN SAINT NAZAIRE
MedGen UID:
924623
Concept ID:
C4284149
Finding
HEMOGLOBIN DEBROUSSE
MedGen UID:
924627
Concept ID:
C4284153
Finding
HEMOGLOBIN KARLSKOGA
MedGen UID:
924629
Concept ID:
C4284155
Finding
HEMOGLOBIN RANCHO MIRAGE
MedGen UID:
924634
Concept ID:
C4284162
Finding
HEMOGLOBIN DENVER
MedGen UID:
924638
Concept ID:
C4284166
Finding
HEMOGLOBIN TYNE
MedGen UID:
924639
Concept ID:
C4284167
Finding
HEMOGLOBIN BREM-SUR-MER
MedGen UID:
924640
Concept ID:
C4284168
Finding
HEMOGLOBIN BARBIZON
MedGen UID:
924642
Concept ID:
C4284170
Finding
HEMOGLOBIN TSUKUMI
MedGen UID:
924643
Concept ID:
C4284171
Finding
HEMOGLOBIN TIZI-OUZOU
MedGen UID:
924644
Concept ID:
C4284172
Finding
HEMOGLOBIN PUTTELANGE
MedGen UID:
924698
Concept ID:
C4284259
Finding
HEMOGLOBIN QUEBEC-CHORI
MedGen UID:
924699
Concept ID:
C4284260
Finding
HEMOGLOBIN 'T LANGE LAND
MedGen UID:
924701
Concept ID:
C4284263
Finding
HEMOGLOBIN ALESHA
MedGen UID:
924704
Concept ID:
C4284266
Finding
HEMOGLOBIN ANTALYA
MedGen UID:
924705
Concept ID:
C4284267
Finding
HEMOGLOBIN AUBAGNE
MedGen UID:
924706
Concept ID:
C4284268
Finding
HEMOGLOBIN BAB-SAADOUN
MedGen UID:
924708
Concept ID:
C4284270
Finding
HEMOGLOBIN WASHTENAW
MedGen UID:
924752
Concept ID:
C4284328
Finding
HEMOGLOBIN DUINO
MedGen UID:
924755
Concept ID:
C4284332
Finding
HEMOGLOBIN SITIA
MedGen UID:
924756
Concept ID:
C4284336
Finding
HEMOGLOBIN TRENTO
MedGen UID:
924766
Concept ID:
C4284347
Finding
HEMOGLOBIN YAIZU
MedGen UID:
924768
Concept ID:
C4284349
Finding
HEMOGLOBIN WATFORD
MedGen UID:
924769
Concept ID:
C4284350
Finding
HEMOGLOBIN REDONDO
MedGen UID:
924789
Concept ID:
C4284420
Finding
HEMOGLOBIN RENERT
MedGen UID:
924791
Concept ID:
C4284422
Finding
HEMOGLOBIN RIO CLARO
MedGen UID:
924792
Concept ID:
C4284423
Finding
HEMOGLOBIN SAALE
MedGen UID:
924795
Concept ID:
C4284427
Finding
HEMOGLOBIN SAGAMI
MedGen UID:
924796
Concept ID:
C4284428
Finding
HEMOGLOBIN BECKMAN
MedGen UID:
924798
Concept ID:
C4284430
Finding
HEMOGLOBIN BADEN
MedGen UID:
924799
Concept ID:
C4284431
Finding
HEMOGLOBIN BRIE COMTE ROBERT
MedGen UID:
924803
Concept ID:
C4284435
Finding
HEMOGLOBIN BUSHEY
MedGen UID:
924806
Concept ID:
C4284438
Finding
HEMOGLOBIN BUZEN
MedGen UID:
924807
Concept ID:
C4284439
Finding
HEMOGLOBIN CALAIS
MedGen UID:
924809
Concept ID:
C4284441
Finding
HEMOGLOBIN CANTERBURY
MedGen UID:
924810
Concept ID:
C4284442
Finding
HEMOGLOBIN CARDARELLI
MedGen UID:
924811
Concept ID:
C4284443
Finding
HEMOGLOBIN CASABLANCA
MedGen UID:
924812
Concept ID:
C4284444
Finding
HEMOGLOBIN MEDICINE LAKE
MedGen UID:
924830
Concept ID:
C4284468
Finding
HEMOGLOBIN HINWIL
MedGen UID:
924836
Concept ID:
C4284480
Finding
HEMOGLOBIN MANUKAU
MedGen UID:
924840
Concept ID:
C4284485
Finding
HEMOGLOBIN ST. FRANCIS
MedGen UID:
924845
Concept ID:
C4284490
Finding
HEMOGLOBIN HOWICK
MedGen UID:
924858
Concept ID:
C4284503
Finding
HEMOGLOBIN TRIPOLI
MedGen UID:
924860
Concept ID:
C4284505
Finding
HEMOGLOBIN TIGRAYE
MedGen UID:
924861
Concept ID:
C4284506
Finding
HEMOGLOBIN VALLETTA
MedGen UID:
924865
Concept ID:
C4284510
Finding
HEMOGLOBIN SANTA CLARA
MedGen UID:
924891
Concept ID:
C4284601
Finding
HEMOGLOBIN SANTANDER
MedGen UID:
924892
Concept ID:
C4284602
Finding
HEMOGLOBIN CHILE
MedGen UID:
924900
Concept ID:
C4284610
Finding
HEMOGLOBIN CLEVELAND
MedGen UID:
924902
Concept ID:
C4284612
Finding
HEMOGLOBIN COIMBRA
MedGen UID:
924903
Concept ID:
C4284613
Finding
HEMOGLOBIN COSTA RICA
MedGen UID:
924906
Concept ID:
C4284616
Finding
HEMOGLOBIN SOUTH MILWAUKEE
MedGen UID:
924950
Concept ID:
C4284746
Finding
HEMOGLOBIN DHONBURI
MedGen UID:
924952
Concept ID:
C4284748
Finding
HEMOGLOBIN GALICIA
MedGen UID:
924957
Concept ID:
C4284753
Finding
HEMOGLOBIN GRAZ
MedGen UID:
924959
Concept ID:
C4284755
Finding
HEMOGLOBIN HAKKARI
MedGen UID:
924960
Concept ID:
C4284756
Finding
HEMOGLOBIN HARROW
MedGen UID:
924990
Concept ID:
C4284897
Finding
HEMOGLOBIN HOKUSETSU
MedGen UID:
924991
Concept ID:
C4284898
Finding
HEMOGLOBIN HRADEC KRALOVE
MedGen UID:
924992
Concept ID:
C4284899
Finding
HEMOGLOBIN ILMENAU
MedGen UID:
924993
Concept ID:
C4284900
Finding
HEMOGLOBIN IRAQ-HALABJA
MedGen UID:
924994
Concept ID:
C4284901
Finding
HEMOGLOBIN JACKSONVILLE
MedGen UID:
924996
Concept ID:
C4284903
Finding
HEMOGLOBIN TERRE HAUTE
MedGen UID:
924997
Concept ID:
C4284904
Finding
HEMOGLOBIN MANHATTAN
MedGen UID:
925010
Concept ID:
C4284922
Finding
HEMOGLOBIN VILLAVERDE
MedGen UID:
925011
Concept ID:
C4284923
Finding
HEMOGLOBIN KOREA
MedGen UID:
925012
Concept ID:
C4284924
Finding
HEMOGLOBIN D (NEATH)
MedGen UID:
925013
Concept ID:
C4284925
Finding
HEMOGLOBIN DIEPPE
MedGen UID:
925014
Concept ID:
C4284926
Finding
HEMOGLOBIN TROLLHAETTAN
MedGen UID:
925015
Concept ID:
C4284927
Finding
HEMOGLOBIN ARTA
MedGen UID:
925016
Concept ID:
C4284928
Finding
HEMOGLOBIN ZENGCHENG
MedGen UID:
925028
Concept ID:
C4284941
Finding
HEMOGLOBIN KOCHI
MedGen UID:
925031
Concept ID:
C4285049
Finding
HEMOGLOBIN KODAIRA
MedGen UID:
925032
Concept ID:
C4285050
Finding
HEMOGLOBIN LA ROCHE-SUR-YON
MedGen UID:
925034
Concept ID:
C4285052
Finding
HEMOGLOBIN TSURUMAI
MedGen UID:
925041
Concept ID:
C4285059
Finding
HEMOGLOBIN VILA REAL
MedGen UID:
925043
Concept ID:
C4285061
Finding
HEMOGLOBIN J (EUROPA)
MedGen UID:
925056
Concept ID:
C4285077
Finding
HEMOGLOBIN BURTON-UPON-TRENT
MedGen UID:
925057
Concept ID:
C4285078
Finding
HEMOGLOBIN TENDE
MedGen UID:
925058
Concept ID:
C4285079
Finding
HEMOGLOBIN ERNZ
MedGen UID:
925059
Concept ID:
C4285080
Finding
HEMOGLOBIN MONT SAINT-AIGNAN
MedGen UID:
925060
Concept ID:
C4285081
Finding
HEMOGLOBIN D (AGRI)
MedGen UID:
925061
Concept ID:
C4285082
Finding
HEMOGLOBIN O (TIBESTI)
MedGen UID:
925062
Concept ID:
C4285083
Finding
HEMOGLOBIN KODAIRA II
MedGen UID:
925063
Concept ID:
C4285084
Finding
HEMOGLOBIN COLIMA
MedGen UID:
925064
Concept ID:
C4285090
Finding
HEMOGLOBIN POCOS DE CALDAS
MedGen UID:
925065
Concept ID:
C4285091
Finding
HEMOGLOBIN S (CAMEROON)
MedGen UID:
925066
Concept ID:
C4285092
Finding
HEMOGLOBIN JAMAICA PLAIN
MedGen UID:
925067
Concept ID:
C4285093
Finding
HEMOGLOBIN ROCKFORD
MedGen UID:
925068
Concept ID:
C4285094
Finding
HEMOGLOBIN GELDROP ST. ANNA
MedGen UID:
925069
Concept ID:
C4285095
Finding
HEMOGLOBIN LA CORUNA
MedGen UID:
925070
Concept ID:
C4285096
Finding
HEMOGLOBIN MOLFETTA
MedGen UID:
925077
Concept ID:
C4285216
Finding
HEMOGLOBIN MUSCAT
MedGen UID:
925079
Concept ID:
C4285218
Finding
HEMOGLOBIN GRENOBLE
MedGen UID:
925091
Concept ID:
C4285232
Finding
HEMOGLOBIN SILVER SPRINGS
MedGen UID:
925092
Concept ID:
C4285233
Finding
HEMOGLOBIN YAHATA
MedGen UID:
925094
Concept ID:
C4285340
Finding
HEMOGLOBIN ZOETERWOUDE
MedGen UID:
925095
Concept ID:
C4285341
Finding
HB NIIGATA
MedGen UID:
934938
Concept ID:
C4310971
Finding
BETA-THALASSEMIA, ASHKENAZI JEWISH TYPE
MedGen UID:
934939
Concept ID:
C4310972
Disease or Syndrome
BETA-THALASSEMIA INTERMEDIA, DOMINANT
MedGen UID:
934940
Concept ID:
C4310973
Disease or Syndrome
HEMOGLOBIN OLD DOMINION
MedGen UID:
934973
Concept ID:
C4311006
Finding
HEMOGLOBIN HT
MedGen UID:
934974
Concept ID:
C4311007
Finding
HEMOGLOBIN HK
MedGen UID:
934975
Concept ID:
C4311008
Finding
HEMOGLOBIN DURHAM-N.C.
MedGen UID:
934976
Concept ID:
C4311009
Finding
HEMOGLOBIN CHORI
MedGen UID:
934977
Concept ID:
C4311010
Finding

Recent clinical studies

Etiology

Tillander J, Hagberg K, Berlin Ö, Hagberg L, Brånemark R
Clin Orthop Relat Res 2017 Dec;475(12):3100-3108. Epub 2017 Sep 22 doi: 10.1007/s11999-017-5507-2. PMID: 28940152Free PMC Article
Bernstein B, Stouder M, Bronfenbrenner E, Chen S, Anderson D
J Foot Ankle Res 2017;10:40. Epub 2017 Aug 25 doi: 10.1186/s13047-017-0222-5. PMID: 28855966Free PMC Article
Wu H, Shen J, Yu X, Fu J, Yu S, Sun D, Xie Z
Injury 2017 Feb;48(2):511-518. Epub 2017 Jan 6 doi: 10.1016/j.injury.2017.01.007. PMID: 28088375
Ashong CN, Raheem SA, Hunter AS, Mindru C, Barshes NR
Surg Infect (Larchmt) 2017 Feb/Mar;18(2):143-148. Epub 2016 Nov 29 doi: 10.1089/sur.2016.165. PMID: 27898266
Schnabel A, Range U, Hahn G, Siepmann T, Berner R, Hedrich CM
Rheumatol Int 2016 Dec;36(12):1737-1745. Epub 2016 Oct 11 doi: 10.1007/s00296-016-3572-6. PMID: 27730289

Diagnosis

Tillander J, Hagberg K, Berlin Ö, Hagberg L, Brånemark R
Clin Orthop Relat Res 2017 Dec;475(12):3100-3108. Epub 2017 Sep 22 doi: 10.1007/s11999-017-5507-2. PMID: 28940152Free PMC Article
Bernstein B, Stouder M, Bronfenbrenner E, Chen S, Anderson D
J Foot Ankle Res 2017;10:40. Epub 2017 Aug 25 doi: 10.1186/s13047-017-0222-5. PMID: 28855966Free PMC Article
Conde-Díaz C, Llenas-García J, Parra Grande M, Terol Esclapez G, Masiá M, Gutiérrez F
J Med Case Rep 2017 Feb 21;11(1):48. doi: 10.1186/s13256-017-1221-7. PMID: 28219414Free PMC Article
Hamahashi K, Uchiyama Y, Kobayashi Y, Watanabe M
J Med Case Rep 2017 Jan 31;11(1):23. doi: 10.1186/s13256-016-1187-x. PMID: 28137303Free PMC Article
Mooney ML, Haidet K, Liu J, Ebraheim NA
Foot Ankle Spec 2017 Feb;10(1):63-68. Epub 2016 Nov 23 doi: 10.1177/1938640016679704. PMID: 27881832

Therapy

Roderick MR, Sen ES, Ramanan AV
Rheumatology (Oxford) 2018 Jan 1;57(1):41-48. doi: 10.1093/rheumatology/kex066. PMID: 28486628
Almangour TA, Fletcher V, Alessa M, Alhifany AA, Tabb D
Am J Case Rep 2017 Dec 9;18:1315-1319. PMID: 29222405Free PMC Article
Conde-Díaz C, Llenas-García J, Parra Grande M, Terol Esclapez G, Masiá M, Gutiérrez F
J Med Case Rep 2017 Feb 21;11(1):48. doi: 10.1186/s13256-017-1221-7. PMID: 28219414Free PMC Article
Wu H, Shen J, Yu X, Fu J, Yu S, Sun D, Xie Z
Injury 2017 Feb;48(2):511-518. Epub 2017 Jan 6 doi: 10.1016/j.injury.2017.01.007. PMID: 28088375
Park H, Byeon HK, Kim HS, Hong JJ, Suk KS
Eur Spine J 2017 May;26(Suppl 1):136-140. Epub 2016 Dec 23 doi: 10.1007/s00586-016-4919-0. PMID: 28012078

Prognosis

Almangour TA, Fletcher V, Alessa M, Alhifany AA, Tabb D
Am J Case Rep 2017 Dec 9;18:1315-1319. PMID: 29222405Free PMC Article
Bernstein B, Stouder M, Bronfenbrenner E, Chen S, Anderson D
J Foot Ankle Res 2017;10:40. Epub 2017 Aug 25 doi: 10.1186/s13047-017-0222-5. PMID: 28855966Free PMC Article
Wu H, Shen J, Yu X, Fu J, Yu S, Sun D, Xie Z
Injury 2017 Feb;48(2):511-518. Epub 2017 Jan 6 doi: 10.1016/j.injury.2017.01.007. PMID: 28088375
Park H, Byeon HK, Kim HS, Hong JJ, Suk KS
Eur Spine J 2017 May;26(Suppl 1):136-140. Epub 2016 Dec 23 doi: 10.1007/s00586-016-4919-0. PMID: 28012078
Ashong CN, Raheem SA, Hunter AS, Mindru C, Barshes NR
Surg Infect (Larchmt) 2017 Feb/Mar;18(2):143-148. Epub 2016 Nov 29 doi: 10.1089/sur.2016.165. PMID: 27898266

Clinical prediction guides

Almangour TA, Fletcher V, Alessa M, Alhifany AA, Tabb D
Am J Case Rep 2017 Dec 9;18:1315-1319. PMID: 29222405Free PMC Article
Bernstein B, Stouder M, Bronfenbrenner E, Chen S, Anderson D
J Foot Ankle Res 2017;10:40. Epub 2017 Aug 25 doi: 10.1186/s13047-017-0222-5. PMID: 28855966Free PMC Article
Bremmer D, Bookstaver B, Cairns M, Lindley K, Durkin M, Koon D, Quidley AM
Surg Infect (Larchmt) 2017 Apr;18(3):368-373. Epub 2017 Feb 27 doi: 10.1089/sur.2016.219. PMID: 28394750
Ashong CN, Raheem SA, Hunter AS, Mindru C, Barshes NR
Surg Infect (Larchmt) 2017 Feb/Mar;18(2):143-148. Epub 2016 Nov 29 doi: 10.1089/sur.2016.165. PMID: 27898266
Hofmann SR, Kubasch AS, Range U, Laass MW, Morbach H, Girschick HJ, Hedrich CM
Rheumatol Int 2016 Jun;36(6):769-79. Epub 2016 Mar 21 doi: 10.1007/s00296-016-3466-7. PMID: 27000045

Recent systematic reviews

Geurts J, Hohnen A, Vranken T, Moh P
Trop Med Int Health 2017 Sep;22(9):1054-1062. Epub 2017 Jul 21 doi: 10.1111/tmi.12921. PMID: 28665557
Hong JPJ, Goh TLH, Choi DH, Kim JJ, Suh HS
Plast Reconstr Surg 2017 Jul;140(1):179-188. doi: 10.1097/PRS.0000000000003460. PMID: 28654608
Mauler F, Wanivenhaus F, Böni T, Berli M
J Foot Ankle Surg 2017 May - Jun;56(3):666-669. doi: 10.1053/j.jfas.2017.01.025. PMID: 28476396
Mooney ML, Haidet K, Liu J, Ebraheim NA
Foot Ankle Spec 2017 Feb;10(1):63-68. Epub 2016 Nov 23 doi: 10.1177/1938640016679704. PMID: 27881832
Inzana JA, Schwarz EM, Kates SL, Awad HA
Biomaterials 2016 Mar;81:58-71. Epub 2015 Dec 18 doi: 10.1016/j.biomaterials.2015.12.012. PMID: 26724454Free PMC Article

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