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

• OMIM:617783

Ontology

Human Disease   ( DOID:0080272 )