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Items: 1 to 20 of 42

1.

Focal segmental glomerulosclerosis

MedGen UID:
449387
Concept ID:
CN043606
Disease or Syndrome
2.

Channelopathies

A variety of neuromuscular conditions resulting from MUTATIONS in ION CHANNELS manifesting as episodes of EPILEPSY; HEADACHE DISORDERS; and DYSKINESIAS. [from MeSH]

MedGen UID:
328427
Concept ID:
C1720983
Disease or Syndrome
3.

FK 506

complex, lipid-soluble, macrocyclic lactone produced by the Japanese soil bacterium Streptomyces tsukubaensis; experimental immunosuppressant which inhibits T-lymphocyte activation and fungal growth by binding to peptidyl prolyl isomerase, forming a complex which interferes with calcium signaling. [from CRISP]

MedGen UID:
149087
Concept ID:
C0729218
Organic Chemical; Pharmacologic Substance
4.

Segmental glomerulosclerosis

MedGen UID:
83080
Concept ID:
C0333497
Disease or Syndrome
5.

Syndrome

A characteristic symptom complex. [from MeSH]

MedGen UID:
11688
Concept ID:
C0039082
Disease or Syndrome
6.

Nephrotic syndrome

A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction. [from NCI]

MedGen UID:
10308
Concept ID:
C0027726
Disease or Syndrome
7.

Hereditary nephritis

A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE. [from MeSH]

MedGen UID:
10305
Concept ID:
C0027706
Disease or Syndrome
8.

Calcium

A basic element found in nearly all organized tissues. It is a member of the alkaline earth family of metals with the atomic symbol Ca, atomic number 20, and atomic weight 40. Calcium is the most abundant mineral in the body and combines with phosphorus to form calcium phosphate in the bones and teeth. It is essential for the normal functioning of nerves and muscles and plays a role in blood coagulation (as factor IV) and in many enzymatic processes. [from MeSH]

MedGen UID:
710
Concept ID:
C0006675
Biologically Active Substance; Element, Ion, or Isotope; Pharmacologic Substance
9.

Poor prognosis

MedGen UID:
548766
Concept ID:
C0278252
Finding
10.

Borries syndrome

MedGen UID:
542920
Concept ID:
C0270677
Disease or Syndrome
11.

Nephrotic syndrome

Nephrotic syndrome is a collection of findings resulting from glomerular dysfunction with an increase in glomerular capillary wall permeability associated with pronounced proteinuria. Nephrotic syndrome refers to the constellation of clinical findings that result from severe renal loss of protein, with Proteinuria and hypoalbuminemia, edema, and hyperlipidemia. [from HPO]

MedGen UID:
504341
Concept ID:
CN000100
Finding
12.

Focal segmental glomerulosclerosis

MedGen UID:
376918
Concept ID:
C1850973
13.

Pathogenesis

The pathologic, physiologic, or biochemical mechanism resulting in the development of a disease or morbid process. [from NCI]

MedGen UID:
195936
Concept ID:
C0699748
Pathologic Function
14.

Mutant

An altered form of an individual, organism, population, or genetic character that differs from the corresponding wild type due to one or more alterations (mutations). [from NCI]

MedGen UID:
109303
Concept ID:
C0596988
Cell or Molecular Dysfunction
15.

Progressive hereditary glomerulonephritis without deafness

MedGen UID:
98012
Concept ID:
C0403443
Disease or Syndrome
16.

Transient

Short-lived and not permanent. This term applies to a phenotypic abnormality that is temporary and of short duration. [from HPO]

MedGen UID:
64403
Concept ID:
C0205374
Temporal Concept
17.

Focal

Area of greatest concentration, attention, or activity; a central point or locus, especially of an infection. [from NCI]

MedGen UID:
61391
Concept ID:
C0205234
Spatial Concept
18.

Glomerulosclerosis

A hardening of the kidney glomerulus caused by scarring of the blood vessels. [from NCI]

MedGen UID:
61248
Concept ID:
C0178664
Disease or Syndrome
19.

Male Urogenital Diseases

Pathological processes of the male URINARY TRACT and the reproductive system (GENITALIA, MALE). [from MeSH]

MedGen UID:
318601
Concept ID:
C1720894
Disease or Syndrome
20.

Female Urogenital Diseases

Pathological processes of the female URINARY TRACT and the reproductive system (GENITALIA, FEMALE). [from MeSH]

MedGen UID:
318599
Concept ID:
C1720887
Disease or Syndrome
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