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Disease Ontology Browser
autosomal dominant dyskeratosis congenita 6 (DOID:0070023)
Alliance: disease page
Synonyms: DKCA6
Alt IDs: OMIM:616553
Definition: A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of ACD on chromosome 16q22.1.


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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory