Optic atrophy 4

Preferred Label : Optic atrophy 4;

Symbol : OPA4;

CISMeF acronym : OPA4;

Type : Phenotype or locus, molecular basis unknown;

Description : For a discussion of genetic heterogeneity of optic atrophy, see OPA1 (165500).;

Prefixed ID : %605293;

Details

Origin ID

605293;

UMLS CUI

C1854430;

Currated CISMeF NLP mapping
- optic atrophy 4 [DO Concept]
- optic atrophy 4 [MeSH concept]
- optic atrophy 4 [MeSH Supplementary Concept]
DO Cross reference
- optic atrophy 4 [DO Concept]
ORDO concept(s)
- Autosomal dominant optic atrophy, classic form [ORDO Disease]
- Genetic optic atrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- optic atrophy 4 [MeSH Supplementary Concept]
- optic atrophy 4 [MeSH concept]

Keyword's position in hierarchy(ies) :

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