focal segmental glomerulosclerosis 9
Go to external page http://purl.obolibrary.org/obo/MONDO_0014539
Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the CRB2 gene. [ MONDO:patterns/disease_series_by_gene ]
Synonyms: CRB2 focal segmental glomerulosclerosis FSGS9 focal segmental glomerulosclerosis type 9 focal segmental glomerulosclerosis 9 focal segmental glomerulosclerosis caused by mutation in CRB2
Term information
- UMLS:C4015555 (MONDO:ncbi_mim2gene_medline)
- OMIM:616220 (MONDO:equivalentTo)
- DOID:0111134 (MONDO:equivalentTo)
- GARD:16070 (OMIM:616220)
gard_rare, rare, nord_rare, clingen
http://purl.obolibrary.org/obo/DOID_0111134
https://omim.org/entry/616220
http://linkedlifedata.com/resource/umls/id/C4015555