Leber hereditary optic neuropathy, modifier of

Preferred Label : Leber hereditary optic neuropathy, modifier of;

Symbol : LOAM;

CISMeF acronym : LOAS;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Lhon, modifier of; Leber optic atrophy, susceptibility to; LOAS;

Inheritance : X-linked;

Prefixed ID : #308905;

Details

Origin ID

308905;

UMLS CUI

C1839891;

Genes related to phenotype
- Prickle planar cell polarity protein 3 [OMIM gene]
HPO term(s)
- Leber optic atrophy [HPO term]
- Optic atrophy [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- Leber hereditary optic neuropathy [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

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