Search Ontology:
Human Disease

nephrotic syndrome type 16

Term ID
DOID:0080272
Synonyms
Definition
A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/25961457
References
Ontology
Human Disease   ( DOID:0080272 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models