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DOID:0110710 - hypotrichosis 13
Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the KRT71 gene on chromosome 12q13.13.
Synonyms: Hypt13, hypotrichosis with woolly hair,
Xenbase Genes :
MONDO:0014390 - hypotrichosis 13 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee