Disease #04358 (FSGS8 (glomerulosclerosis, focal segmental, type 8 (FSGS-8)), OMIM:616032)

Official abbreviation FSGS8
Name glomerulosclerosis, focal segmental, type 8 (FSGS-8)
OMIM ID 616032
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ANLN
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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