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DOID:0110034 - X-linked Alport syndrome
Disease Ontology Definition:An Alport syndrome that has_material -basis_in mutation in the gene encoding the alpha-5 chain of basement membrane collagen type IV (COL4A5).
Synonyms: ATS, nephropathy and deafness, X-linked,
Echinobase Genes :
MIM:301050 - alport syndrome, x-linked; ats |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Alport syndrome (is_a)