has characteristic has characteristic Autosomal dominant inheritance autosomal dominant disease hereditary optic neuropathy autosomal dominant optic atrophy https://github.com/monarch-initiative/mondo/issues/9831 2026-05-01 optic atrophy, autosomal dominant DOA ADOA MESH:D029241 dominant optic atrophy UMLS:C4551508 MEDGEN:1647918 NCIT:C84577 MONDO:0020250 GARD:0011972 Orphanet:98672 This term is scheduled for obsoletion based on the fact that it is a grouping class. After obsoletion, this term will not have a replacement ID, but one could consider the following term: - SCTID:2065009 An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss. hereditary optic atrophy