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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 the DKC1 gene on chromosome Xq28.
Synonyms: DKCX, Zinsser-Cole-Engman syndrome,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0010584 - dyskeratosis congenita, X-linked |
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)