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DOID:0110698 - hypotrichosis 1
Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the APCDD1 gene on chromosome 18p11.22.
Synonyms: Hhs, Hts, Hypt1, hereditary generalized hypotrichosis simplex,
Echinobase Genes : LOC581394
MIM:605389 - hypotrichosis 1; hypt1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee