ZFIN Human Disease: nephrotic syndrome type 11

OBO ID: DOID:0080385

Term Name:	nephrotic syndrome type 11		Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome characterized by onset in the first decade of life of steroid resistant progressive renal disease that has_material_basis_in homozygous or compound heterozygous mutation in the NUP107 gene on chromosome 12q15. https://www.ncbi.nlm.nih.gov/pubmed/26411495
References:	OMIM:616730
Ontology:	Human Disease ( DOID:0080385 )

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 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NUP107	nup107	Nephrotic syndrome, type 11	616730

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None