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Disease Ontology Browser
autosomal recessive dyskeratosis congenita 3 (DOID:0070019)
Alliance: disease page
Synonyms: DKCB3
Alt IDs: OMIM:613988
Definition: A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of WRAP53 on chromosome 17p13.1.

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
03/14/2023
MGI 6.22 		The Jackson Laboratory