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DOID:0070025 - X-linked dyskeratosis congenita
Disease Ontology Definition:A dyskeratosis congenita that has_material_basis_in an X-linked recessive mutation of DKC1 on chromosome Xq28.
Synonyms: DKCX, Zinsser-Cole-Engman syndrome
Echinobase Genes : dkc1
MIM:305000 - dyskeratosis congenita, x-linked; dkcx |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
dyskeratosis congenita (is_a)