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DOID:0110835 - Usher syndrome type 1H
Disease Ontology Definition:An Usher syndrome type 1 that has_material_basis_in variation in the chromosome region 15q22-q23.
Synonyms: USH1H, Usher syndrome type IH,
Xenbase Genes :
MONDO:0012968 - Usher syndrome type 1H |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Usher syndrome type 1 (is_a)