Dystonia 15, myoclonic

Preferred Label : Dystonia 15, myoclonic;

Symbol : DYT15;

CISMeF acronym : DYT15;

Type : Phenotype or locus, molecular basis unknown;

Description : For general phenotypic information and a discussion of genetic heterogeneity of myoclonic dystonia, see 159900.;

Inheritance : Autosomal dominant;

Prefixed ID : %607488;

Details

Origin ID

607488;

UMLS CUI

C1843786;

Currated CISMeF NLP mapping
- Dystonia 15, myoclonic [MeSH concept]
- Myoclonic dystonia 15 [ORDO Disease]
- dystonia 15, myoclonic [MeSH Supplementary Concept]
- myoclonic dystonia 15 [DO Concept]
DO Cross reference
- myoclonic dystonia 15 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dystonia [HPO term]
- Heterogeneous [HPO term]
- Myoclonus [HPO term]
- Writer's cramp [HPO term]
ORDO concept(s)
- Myoclonic dystonia 15 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dystonia 15, myoclonic [MeSH concept]
- Myoclonic dystonia 15 [ORDO Disease]
- dystonia 15, myoclonic [MeSH Supplementary Concept]
- dystonia 15, myoclonic [ORDO Gene]
- myoclonic dystonia 15 [DO Concept]

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