ZFIN Human Disease: nephrotic syndrome type 13

OBO ID: DOID:0080381

Term Name:	nephrotic syndrome type 13		Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome characterized by early onset of steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis that has_material_basis_in homozygous mutation in the NUP205 gene on chromosome 7q33. https://www.ncbi.nlm.nih.gov/pubmed/26878725
References:	OMIM:616893
Ontology:	Human Disease ( DOID:0080381 )

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 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NUP205	nup205	?Nephrotic syndrome, type 13	616893

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None