Immunodeficiency 105, severe combined

Preferred Label : Immunodeficiency 105, severe combined;

Symbol : IMD105;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Scid, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive; Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive;

Prefixed ID : #619924;

Détails

Origin ID

619924;

UMLS CUI

C5677005;

Genes related to phenotype
- Protein-tyrosine phosphatase, receptor-type, C [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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