Term Name: | nephronophthisis 19 |
---|---|
Synonyms: | NPHP19 |
Definition: | A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the DCDC2 gene on chromosome 6p22. |
Ontology: | Human Disease [DOID:0111126] ( DOID:0111126 ) |