DO_rare_slim has material basis in autosomal dominant disease ocular pterygium-digital keloid dysplasia syndrome UMLS_CUI:C5975613 MIM:621091 A syndrome characterized by aggressive circumferential ingrowth of conjunctiva beginning in early childhood that is resistant to treatment, ultimately covering the cornea and resulting in loss of vision, and digital keloid formation after minor trauma that has_material_basis_in heterozygous mutation in the PDGFRB gene on chromosome 5q32. OPDKD disease_ontology DOID:0070821 MIM:621091 UMLS_CUI:C5975613 syndrome autosomal dominant inheritance