ZFIN Human Disease: nephrotic syndrome type 14

OBO ID: DOID:0080265

OBO ID: DOID:0080265

Term Name:	nephrotic syndrome type 14	Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the sphingosine-1-phosphate lyase 1 (SGPL1) gene on chromosome 10q21. (3)
References:	OMIM:617575
Ontology:	Human Disease ( DOID:0080265 )

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 14 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SGPL1	sgpl1	RENI syndrome	617575

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None