Dystonia 13, torsion, autosomal dominant

Preferred Label : Dystonia 13, torsion, autosomal dominant;

Symbol : DYT13;

CISMeF acronym : DYT13;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %607671;

Details

Origin ID

607671;

UMLS CUI

C1843264;

Currated CISMeF NLP mapping
- Primary dystonia type 13 (disorder) [SNOMED CT concept]
- Primary dystonia, DYT13 type [ICD-11 More detail]
- Primary dystonia, DYT13 type [ORDO Disease]
- dystonia 13, torsion [MeSH Supplementary Concept]
- dystonia 13, torsion [MeSH concept]
- torsion dystonia 13 [DO Concept]
DO Cross reference
- torsion dystonia 13 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Blepharospasm [HPO term]
- Cranial dystonia [HPO term]
- Limb dystonia [HPO term]
- Oromandibular dystonia [HPO term]
- Torsion dystonia [HPO term]
- Torticollis [HPO term]
- Tremor [HPO term]
- Writer's cramp [HPO term]
ORDO concept(s)
- Primary dystonia, DYT13 type [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Primary dystonia type 13 (disorder) [SNOMED CT concept]
- Primary dystonia, DYT13 type [ORDO Disease]
- dystonia 13, torsion [MeSH Supplementary Concept]
- dystonia 13, torsion [MeSH concept]
- torsion dystonia 13 [DO Concept]

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