dystonia 17, torsion, autosomal recessive

Preferred Label : dystonia 17, torsion, autosomal recessive;

Origin ID

C567319;

UMLS CUI

C2676281;

Currated CISMeF NLP mapping
- Dystonia 17, torsion, autosomal recessive [OMIM Phenotype]
- Primary dystonia DYT17 type (disorder) [SNOMED CT concept]
- Primary dystonia, DYT17 type [ORDO Disease]
- torsion dystonia 17 [DO Concept]
MeSH term(s) associated for indexing
- dystonic disorders [MeSH Descriptor]
Record concept(s)
- dystonia 17, torsion, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dystonia 17, torsion, autosomal recessive [OMIM Phenotype]