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DOID:0110706 - hypotrichosis 9
Disease Ontology Definition:A hypotrichosis that has_material_basis_in an autosomal recessive mutation on chromosome 10q11.23-q22.3.
Synonyms: Hypt9,
Xenbase Genes :
MONDO:0013649 - hypotrichosis 9 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hypotrichosis (is_a)