ZFIN Human Disease: nephrotic syndrome type 7

OBO ID: DOID:0080388

Term Name:	nephrotic syndrome type 7		Search Ontology:
Synonyms:	Ig-mediated membranoproliferative glomerulonephritis Ig-mediated MPGN immunoglobulin-mediated membranoproliferative glomerulonephritis Immunoglobulin-mediated MPGN nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis
Definition:	A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22. https://www.ncbi.nlm.nih.gov/pubmed/23274426
References:	OMIM:615008 ORDO:329903
Ontology:	Human Disease ( DOID:0080388 )

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 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DGKE	dgke	{Hemolytic uremic syndrome, atypical, susceptibility to, 7}	615008
		Nephrotic syndrome, type 7	615008

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None