has material basis in germline mutation in CLCC1 retinitis pigmentosa 32 https://rarediseases.info.nih.gov/diseases/10395/retinitis-pigmentosa-32 https://www.malacards.org/card/retinitis_pigmentosa_32 retinitis pigmentosa 32 MESH:C563689 MEDGEN:322781 GARD:0010395 MONDO:0012363 UMLS:C1835927 retinitis pigmentosa type 32 OMIM:609913 A retinitis pigmentosa that has material basis in variation in the chromosome region 1p21.3-p13.3. DOID:0110355 RP32 retinitis pigmentosa