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DOID:0070018 - autosomal dominant dyskeratosis congenita 3
Disease Ontology Definition:A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of TINF2 on chromosome 14q12.
Synonyms: DKCA3,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
dyskeratosis congenita (is_a)