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Disease Ontology Browser
X-linked dyskeratosis congenita (DOID:0070025)
Alliance: disease page
Synonyms: DKCX; Zinsser-Cole-Engman syndrome
Alt IDs: OMIM:305000
Definition: A dyskeratosis congenita that has_material_basis_in an X-linked recessive mutation of the DKC1 gene on chromosome Xq28.

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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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last database update
MGI 6.13
The Jackson Laboratory