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autosomal dominant optic atrophy

^ http://purl.obolibrary.org/obo/MONDO_0020250

An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss. [ NCIT:C84577 ]

Term info

database cross reference
  • SCTID:2065009 (MONDO:equivalentTo)
  • Orphanet:98672 (MONDO:equivalentTo)
  • MESH:D029241 (Orphanet:98672/e)
  • GARD:0011972 (MONDO:equivalentTo)
  • NCIT:C84577 (MONDO:equivalentTo)
  • UMLS:C0338508 (Orphanet:98672/e)
Subsets

disease_grouping, ordo_group_of_disorders

abbreviation
ADOA [ Orphanet:98672 ]

abbreviation
DOA [ Orphanet:98672 ]

definition

An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_98672, http://purl.obolibrary.org/obo/NCIT_C84577, http://identifiers.org/snomedct/2065009, http://linkedlifedata.com/resource/umls/id/C0338508, http://identifiers.org/mesh/D029241

has exact synonym

DOA, ADOA, optic atrophy, autosomal dominant

has related synonym

dominant optic atrophy

id

MONDO:0020250