has characteristic has characteristic has material basis in germline mutation in COL4A5 X-linked inheritance X-linked disease X-linked Alport syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/alport_syndrome_1_x_linked https://www.malacards.org/card/x_linked_alport_syndrome DOID:0110034 ATS MEDGEN:1648433 UMLS:C4746986 X-linked form of Alport syndrome. congenital hereditary hematuria hemorrhagic hereditary nephritis nephropathy and deafness, X-linked Orphanet:88917 Alport syndrome, X-linked Alport syndrome 1, X-linked, X-linked dominant MONDO:0010520 X-linked Alport syndrome MedDRA:10001843 SCTID:717768004 hemorrhagic familial nephritis OMIM:301050 GARD:0016774 Alport syndrome