Episodic ataxia, type 7

Preferred Label : Episodic ataxia, type 7;

Symbol : EA7;

CISMeF acronym : EA7;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of episodic ataxia, see EA1 (160120).;

Inheritance : Autosomal dominant;

Prefixed ID : %611907;

Details

Origin ID

611907;

UMLS CUI

C2677843;

Currated CISMeF NLP mapping
- Episodic ataxia type 7 [ICD-11 More detail]
- Episodic ataxia type 7 [ORDO Disease]
- Episodic ataxia type 7 (disorder) [SNOMED CT concept]
- episodic ataxia type 7 [DO Concept]
- episodic ataxia, type 7 [MeSH concept]
- episodic ataxia, type 7 [MeSH Supplementary Concept]
DO Cross reference
- episodic ataxia type 7 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dysarthria [HPO term]
- Episodic ataxia [HPO term]
- Muscle weakness [HPO term]
- Vertigo [HPO term]
- Weakness [HPO term]
ORDO concept(s)
- Episodic ataxia type 7 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Episodic ataxia type 7 [ORDO Disease]
- Episodic ataxia type 7 [ICD-11 More detail]
- Episodic ataxia type 7 (disorder) [SNOMED CT concept]
- episodic ataxia type 7 [DO Concept]
- episodic ataxia, type 7 [MeSH Supplementary Concept]
- episodic ataxia, type 7 [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients