DO_rare_slim has material basis in autosomal dominant disease diffuse cystic renal dysplasia disease_ontology MIM:601331 GARD:4658 DOID:0111682 A cystic kidney disease characterized by nonsyndromic diffuse cystic dysplasia of the kidneys that has_material_basis_in heterozygous mutation in the BICC1 gene on chromosome 10q21.1. The same mutation maybe found in unaffected parents suggesting incomplete penetrance of the disorder or that additional environmental factors are required for development of the disorder. CYSRD renal dysplasia diffuse cystic susceptibility to cystic renal dysplasia cystic kidney disease autosomal dominant inheritance