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DOID:0110707 - hypotrichosis 10
Disease Ontology Definition:A hypotrichosis that has_material_basis_in an autosomal recessive mutation on chromosome 7p22.3-p21.3.
Synonyms: Hypt10,
Xenbase Genes :
MONDO:0013650 - hypotrichosis 10 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee