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Results: 10

1.

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
2.

Epithelial proliferation

MedGen UID:
569543
Concept ID:
C0334097
Pathologic Function
3.

Combined immunodeficiency

MedGen UID:
505803
Concept ID:
CN004782
Finding
4.

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
5.

Immunodeficiency

MedGen UID:
505335
Concept ID:
CN002471
Finding
6.

Proliferation

Growth and reproduction of new similar forms, e.g. cells, buds, or offspring. [from NCI]

MedGen UID:
137720
Concept ID:
C0334094
Pathologic Function
7.

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
8.

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
9.

Murine

MedGen UID:
108834
Concept ID:
C0591833
Pharmacologic Substance
10.

Lymphoma confined to mucosa AND/OR submucosa

MedGen UID:
723975
Concept ID:
C1302399
Finding

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