autosomal dominant dyskeratosis congenita 3 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant dyskeratosis congenita 3 (DOID:0070018)
Alliance: disease page
Synonyms: DKCA3
Alt IDs: OMIM:613990
Definition: A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of the TINF2 gene on chromosome 14q12.

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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