DISEASES

Disease-gene associations mined from literature

Human genes for nephronophthisis 19

Nephronophthisis 19 [DOID:0111126]

A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the DCDC2 gene on chromosome 6p22.

Synonyms:  nephronophthisis 19,  DOID:0111126,  NPHP19