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DOID:0110709 - hypotrichosis 12
Disease Ontology Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the RPL21 gene on chromosome 13q12.2.
Synonyms: Hypt12,
Xenbase Genes : rpl21
MONDO:0014384 - hypotrichosis 12 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee