optic atrophy 6

Preferred Label : optic atrophy 6;

MeSH synonym : optic atrophy, congenital or early infantile, autosomal recessive;

Origin ID

C537127;

UMLS CUI

C1850281;

CISMeF manual mappings
- Autosomal recessive optic atrophy, OPA6 type [ORDO Disease]
Currated CISMeF NLP mapping
- Optic atrophy 6 [OMIM Phenotype]
- optic atrophy 6 [DO Concept]
MeSH term(s) associated for indexing
- optic atrophies, hereditary [MeSH Descriptor]
Record concept(s)
- Optic atrophy 6 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive optic atrophy, OPA6 type [ORDO Disease]
- Optic atrophy 6 [OMIM Phenotype]