WormBase Tree Display for DO_term: DOID:0080272

DOID:0080272 Name: nephrotic syndrome type 16
  Status: Valid
  Definition: A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13.
  Parent: Is_a: DOID:2590
      DOID:0050737
  DB_info: Database: OMIM disease 617783
  Attribute_of: Gene_by_orthology: WBGene00006882