has characteristic has characteristic has material basis in germline mutation in DCN hereditary disease congenital stromal corneal dystrophy https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/corneal_dystrophy_congenital_stromal MEDGEN:400601 icd11.foundation:1796933876 MESH:C566452 ICD9:371.56 CSCD GARD:0016943 DOID:0060445 MONDO:0012401 congenital hereditary stromal dystrophy congenital stromal corneal dystrophy Witschel dystrophy Orphanet:101068 UMLS:C1864738 SCTID:702359002 Congenital stromal corneal dystrophy (CSCD) is an extremely rare form of stromal corneal dystrophy characterized by opaque flaky or feathery clouding of the corneal stroma, and moderate to severe visual loss. OMIM:610048 corneal dystrophy, congenital stromal stromal corneal dystrophy congenital