ZFIN Human Disease: nephrotic syndrome type 8

OBO ID: DOID:0080389

Term Name:	nephrotic syndrome type 8		Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome characterized by neonatal or early childhood onset steroid resistant renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGDIA gene on chromosome 17q25. (2)
References:	OMIM:615244
Ontology:	Human Disease ( DOID:0080389 )

Relationships

is a type of:	autosomal recessive disease familial nephrotic syndrome autosomal recessive disease familial nephrotic syndrome Show first 5 Terms

OTHER nephrotic syndrome type 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ARHGDIA	arhgdia	Nephrotic syndrome, type 8	615244

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None