Leber-like hereditary optic neuropathy, autosomal recessive 2

Preferred Label : Leber-like hereditary optic neuropathy, autosomal recessive 2;

Symbol : LHONAR2;

Type : Phenotype, molecular basis known;

Prefixed ID : #620569;

Details

Origin ID

620569;

UMLS CUI

C5882713;

Genes related to phenotype
- Nadh-ubiquinone oxidoreductase fe-s protein 2 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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