Search Ontology:
Human Disease

nephrotic syndrome type 19

Term ID
DOID:0080394
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
Ontology
Human Disease   ( DOID:0080394 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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