Nystagmus, hereditary vertical

Preferred Label : Nystagmus, hereditary vertical;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %164150;

Details

Origin ID

164150;

UMLS CUI

C1834078;

Automatic exact mappings (from CISMeF team)
- Congenital idiopathic nystagmus [ORDO Disease]
Currated CISMeF NLP mapping
- Hereditary vertical nystagmus [MeSH concept]
- hereditary vertical nystagmus [MeSH Supplementary Concept]
HPO term(s)
- Abnormal vestibulo-ocular reflex [HPO term]
- Ataxia [HPO term]
- Autosomal dominant inheritance [HPO term]
- Vertical nystagmus [HPO term]
ORDO concept(s)
- Congenital idiopathic nystagmus [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary vertical nystagmus [MeSH concept]
- hereditary vertical nystagmus [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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