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Disease Ontology Browser
adenosine deaminase deficiency (DOID:5810)
Alliance: disease page
Synonyms: ADA
Alt IDs: OMIM:102700, ICD10CM:D81.30, NCI:C3962, UMLS_CUI:C0268124
Definition: A severe combined immunodeficiency that is caused by a defective enzyme, adenosine deaminase (ADA), necessary for the breakdown of purines. Lack of ADA causes accumulation of dATP.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory