optic atrophy and cataract, autosomal dominant

Preferred Label : optic atrophy and cataract, autosomal dominant;

MeSH synonym : optic atrophy, cataract, and neurologic disorder; optic atrophy 3, autosomal dominant; Opa3, autosomal dominant;

Details

Origin ID

C537128;

UMLS CUI

C1833809;

Currated CISMeF NLP mapping
- Autosomal dominant optic atrophy and cataract [ICD-11 More detail]
- Autosomal dominant optic atrophy and cataract [ORDO Disease]
- Autosomal dominant optic atrophy and cataract (disorder) [SNOMED CT concept]
- Optic atrophy 3, autosomal dominant [OMIM Phenotype]
- optic atrophy 3 [DO Concept]
DO Cross reference
- optic atrophy 3 [DO Concept]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- optic atrophies, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal dominant optic atrophy and cataract [ORDO Disease]
Record concept(s)
- Optic atrophy and cataract, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant optic atrophy and cataract [ORDO Disease]
- Autosomal dominant optic atrophy and cataract [ICD-11 More detail]
- Autosomal dominant optic atrophy and cataract (disorder) [SNOMED CT concept]
- Autosomal dominant optic atrophy and peripheral neuropathy [ORDO Disease]
- Optic atrophy 3, autosomal dominant [OMIM Phenotype]
- optic atrophy 3 [DO Concept]

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