MeSH Browser

MeSH Supplementary: Segmental glomerulosclerosis
Unique ID: C538457
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538457
Entry Term(s): FSGS1; Focal sclerosis with hyalinosis; Focal segmental glomerulosclerosis 1; Glomerulosclerosis, Focal Segmental, 1
Registry Number: 0
Heading Mapped to: *Glomerulosclerosis, Focal Segmental
Frequency: 71
Note: A pathologic finding in several renal disorders that manifest clinically as PROTEINURIA and progressive decline in renal function. Some patients develop NEPHROTIC SYNDROME (OMIM: 256300), but others may only have proteinuria in the nephrotic syndrome range. Autosomal dominant mutations in the ACTN4 gene have been identified in some cases. OMIM: 603278
Date of Entry: 2010/08/25
Revision Date: 2019/04/01

Segmental glomerulosclerosis MeSH Supplementary Concept Data 2024