Nystagmus, myoclonic

Preferred Label : Nystagmus, myoclonic;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked dominant; ? same as simple nystagmus (310700);

Prefixed ID : 310800;

Details

Origin ID

310800;

UMLS CUI

C1839579;

Automatic exact mappings (from CISMeF team)
- Congenital idiopathic nystagmus [ORDO Disease]
Currated CISMeF NLP mapping
- nystagmus, myoclonic [MeSH concept]
- nystagmus, myoclonic [MeSH Supplementary Concept]
HPO term(s)
- Myoclonus [HPO term]
- Nystagmus [HPO term]
- X-linked dominant inheritance [HPO term]
ORDO concept(s)
- Congenital idiopathic nystagmus [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- nystagmus, myoclonic [MeSH Supplementary Concept]
- nystagmus, myoclonic [MeSH concept]

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