Optic atrophy with demyelinating disease of cns

Preferred Label : Optic atrophy with demyelinating disease of cns;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant; ? same as Leber optic atrophy (535000);

Prefixed ID : 165200;

Details

Origin ID

165200;

UMLS CUI

C1833830;

Currated CISMeF NLP mapping
- optic atrophy with demyelinating disease of CNS [MeSH concept]
- optic atrophy with demyelinating disease of CNS [MeSH Supplementary Concept]
DO Cross reference
- Leber hereditary optic neuropathy with demyelinating disease of CNS [DO Concept]
HPO term(s)
- Ataxia [HPO term]
- Autosomal dominant inheritance [HPO term]
- CNS demyelination [HPO term]
- Demyelination [HPO term]
- Dysarthria [HPO term]
- Hemiparesis [HPO term]
- Optic atrophy [HPO term]
- Optic neuritis [HPO term]
- Peripheral demyelination [HPO term]
ORDO concept(s)
- Leber plus disease [ORDO Disease]
See also inter- (CISMeF)
- Leber plus disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- optic atrophy with demyelinating disease of CNS [MeSH Supplementary Concept]
- optic atrophy with demyelinating disease of CNS [MeSH concept]

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