ZFIN Human Disease: nephrotic syndrome type 19

OBO ID: DOID:0080394

OBO ID: DOID:0080394

Term Name:	nephrotic syndrome type 19	Search Ontology:
Synonyms:
Definition:	A familial nephrotic syndrome that has_material_basis_in compound heterozygous mutation in the NUP160 gene on chromosome 11p11. https://www.ncbi.nlm.nih.gov/pubmed/30179222
References:	OMIM:618178
Ontology:	Human Disease ( DOID:0080394 )

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 19 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NUP160	nup160	?Nephrotic syndrome, type 19	618178

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None