Term info
database cross reference
- MESH:D015418 (MONDO:equivalentTo)
- OMIMPS:165500 (MONDO:equivalentTo)
- NCIT:C34864 (MONDO:equivalentTo)
- SCTID:26360005 (MONDO:equivalentTo)
- UMLS:C0029125 (NCIT:C34864)
definition
A family of inherited disorders characterized by progressive loss of vision secondary to death of the retinal ganglion cell axons that comprise the optic nerve.
exactMatch
http://purl.obolibrary.org/obo/NCIT_C34864, https://omim.org/phenotypicSeries/PS165500, http://identifiers.org/snomedct/26360005, http://linkedlifedata.com/resource/umls/id/C0029125, http://identifiers.org/mesh/D015418
has exact synonym
hereditary optic atrophy
has related synonym
optic atrophy, hereditary, atrophy, hereditary optic, hereditary optic Atrophies, Atrophies, hereditary optic
id
MONDO:0043878