About   Help   FAQ
Disease Ontology Browser
dyskeratosis congenita (DOID:2729)
Alt IDs: OMIM:127550, OMIM:224230, OMIM:305000, OMIM:613987, OMIM:613988, OMIM:613989, OMIM:613990, OMIM:615190, MESH:D019871, NCI:C111802, ORDO:1775, UMLS_CUI:C0265965
Definition: A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer.

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/18/2017
MGI 6.08
The Jackson Laboratory