ZFIN Human Disease: nephrotic syndrome type 15

OBO ID: DOID:0080271

OBO ID: DOID:0080271

Term Name:	nephrotic syndrome type 15	Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the MAGI2 gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/27932480
References:	OMIM:617609
Ontology:	Human Disease ( DOID:0080271 )

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 15 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MAGI2	magi2a magi2b	Nephrotic syndrome, type 15	617609

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None