autosomal dominant optic atrophy plus syndrome https://www.malacards.org/card/autosomal_dominant_optic_atrophy DOA+ optic atrophy - deafness- polyneuropathy - myopathy icd11.foundation:1149710475 optic atrophy type 8 Orphanet:1215 Autosomal dominant optic atrophy plus syndrome (ADOA plus) is a variant of autosomal dominant optic atrophy (ADOA) associating the typical optic atrophy with other extra-ocular manifestations such as sensorineural deafness, myopathy, chronic progressive external ophthalmoplegia, ataxia and peripheral neuropathy. More rarely, other manifestations have been associated with this condition, such as spastic paraplegia, multiple-sclerosis like illness. dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy DOID:0111340 Treft-Sanborn-Carey syndrome optic atrophy-deafness-polyneuropathy-myopathy syndrome SCTID:715374003 MONDO:0014720 GARD:0005243 autosomal dominant optic atrophy mitochondrial disease