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Results: 1 to 20 of 32

1.

brand name of imidacloprid insecticide [from CHV]

MedGen UID:
137141
Concept ID:
C0308269
2.

Combined immunodeficiency

MedGen UID:
505803
Concept ID:
CN004782
Finding
3.

Immunodeficiency

MedGen UID:
505335
Concept ID:
CN002471
Finding
4.

Immunodeficiency

Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. [from MeSH]

MedGen UID:
7034
Concept ID:
C0021051
Disease or Syndrome
5.

X-Linked Severe Combined Immunodeficiency

MedGen UID:
444080
Concept ID:
C2931540
Disease or Syndrome
6.

Severe combined immunodeficiency disease

group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels; it is inherited as an X-linked or autosomal recessive defect; about half of the patients with autosomal recessive SCID are deficient in the enzyme adenosine deaminase. [from CRISP]

MedGen UID:
88328
Concept ID:
C0085110
Disease or Syndrome
7.

Pneumonia

Inflammation of any part, segment or lobe, of the lung parenchyma. [from MeSH]

MedGen UID:
10813
Concept ID:
C0032285
Disease or Syndrome
8.

T cell subsets

MedGen UID:
748541
Concept ID:
C2362651
Finding
9.

Recurrent pneumonia

An increased susceptibility to pneumonia as manifested by a history of recurrent episodes of pneumonia. [from HPO]

MedGen UID:
505924
Concept ID:
CN005690
Finding
10.

Severe combined immunodeficiency

Severe combine immunodeficiency (SCID) is a primary immune deficiency that is characterized by a severe defect in both the T- and B-lymphocyte systems. [from HPO]

MedGen UID:
505637
Concept ID:
CN003925
Finding
11.

Pneumonia

Inflammation of any part of the lung parenchyma. [from HPO]

MedGen UID:
505095
Concept ID:
CN001891
Finding
12.

X-linked severe combined immunodeficiency

X-linked severe combined immunodeficiency (X-SCID) is a combined cellular and humoral immunodeficiency caused by mutations in IL2RG. In typical X-SCID lack of IL2RG function results in near complete absence of T and natural killer (NK) lymphocytes and nonfunctional B lymphocytes. X-SCID is almost universally fatal in the first two years of life unless reconstitution of the immune system is achieved through bone marrow transplant or gene therapy. In the absence of family history of X-SCID and prior to newborn screening for X-SCID, most males with typical X-SCID come to medical attention between ages three and six months. During the first year of life nearly all untreated males with X-SCID exhibit failure to thrive, oral/diaper candidiasis, absent tonsils and lymph nodes, recurrent infections, infections with opportunistic organisms such as Pneumocystis, and persistence of infections despite conventional treatment. Additional common features include rashes, diarrhea, cough and congestion, fevers, pneumonia, sepsis, and other severe bacterial infections. Males with atypical X-SCID may have immune dysregulation and autoimmunity associated with rashes, gastrointestinal malabsorption, and short stature. [from GeneReviews]

MedGen UID:
220906
Concept ID:
C1279481
Disease or Syndrome
13.

MedGen UID:
195802
Concept ID:
C0694550
14.

Severe

A term used to describe cells that look abnormal under a microscope. These cells are more likely to grow and spread quickly than cells in low-grade cancer or in growths that may become cancer. [from NCI]

MedGen UID:
104640
Concept ID:
C0205082
15.

X-linked inheritance

MedGen UID:
66838
Concept ID:
C0241764
16.

DNA Repair-Deficiency Disorders

Disorders resulting from defective DNA REPAIR processes or the associated cellular responses to DNA DAMAGE. [from MeSH]

MedGen UID:
327583
Concept ID:
C1563696
Disease or Syndrome
17.

Nutritional and Metabolic Diseases

A collective term for nutritional disorders resulting from poor absorption or nutritional imbalance, and metabolic disorders resulting from defects in biosynthesis (ANABOLISM) or breakdown (CATABOLISM) of endogenous substances. [from MeSH]

MedGen UID:
45164
Concept ID:
C0028715
Disease or Syndrome
18.

Metabolic Diseases

Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) [from MeSH]

MedGen UID:
44376
Concept ID:
C0025517
Disease or Syndrome
19.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Diseases existing at birth and often before birth, or that develop during the first month of life (INFANT, NEWBORN, DISEASES), regardless of causation. Of these diseases, those characterized by structural deformities are termed CONGENITAL ABNORMALITIES. [from MeSH]

MedGen UID:
14319
Concept ID:
C0027612
Disease or Syndrome
20.

Neonatal disorder

A non-neoplastic or neoplastic disorder which occurs during the neonatal period. [from NCI]

MedGen UID:
9460
Concept ID:
C0021290
Disease or Syndrome

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