autosomal dominant optic atrophy
autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss
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autosomal dominant optic atrophy
Summary
autosomal dominant optic atrophy is a class of disease[1].
Key Facts
- autosomal dominant optic atrophy's instance of is recorded as class of disease[2].
- autosomal dominant optic atrophy's subclass of is recorded as hereditary optic atrophy[3].
- autosomal dominant optic atrophy's subclass of is recorded as optic atrophy[4].
- autosomal dominant optic atrophy's subclass of is recorded as nervous system heredodegenerative disease[5].
- autosomal dominant optic atrophy's subclass of is recorded as eye degenerative disease[6].
- autosomal dominant optic atrophy's Commons category is recorded as Autosomal dominant optic atrophy[7].
- autosomal dominant optic atrophy's MeSH descriptor ID is recorded as D029241[8].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C10.292.700.225.500.100[9].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C10.574.500.662.100[10].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C11.270.564.100[11].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C11.640.451.451.100[12].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C16.320.290.564.100[13].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C16.320.400.630.100[14].
- autosomal dominant optic atrophy's MeSH tree code is recorded as C18.452.660.665[15].
- autosomal dominant optic atrophy's Orphanet ID is recorded as 98672[16].
- autosomal dominant optic atrophy's NCI Thesaurus ID is recorded as C84577[17].
- autosomal dominant optic atrophy's health specialty is recorded as neurology[18].
- autosomal dominant optic atrophy's health specialty is recorded as ophthalmology[19].
- autosomal dominant optic atrophy's health specialty is recorded as medical genetics[20].
- autosomal dominant optic atrophy's health specialty is recorded as endocrinology[21].
- autosomal dominant optic atrophy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98672[22].
- autosomal dominant optic atrophy's UMLS CUI is recorded as C0338508[23].
- autosomal dominant optic atrophy's UMLS CUI is recorded as C4551508[24].
- autosomal dominant optic atrophy's ICD-10-CM is recorded as H47.2[25].
- autosomal dominant optic atrophy's GARD rare disease ID is recorded as 11972[26].