ZFIN Human Disease: nephrotic syndrome type 10

OBO ID: DOID:0080386

Term Name:	nephrotic syndrome type 10		Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome characterized by early childhood onset that has_material_basis_in homozygous or compound heterozygous mutation in the EMP2 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/24814193
References:	OMIM:615861
Ontology:	Human Disease ( DOID:0080386 )

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 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EMP2	emp2	Nephrotic syndrome, type 10	615861

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None