Search Ontology:
Human Disease
dystonia 25
- Term ID
- DOID:0090055
- Synonyms
-
- Definition
- A multifocal dystonia that is characterized by cervical, laryngeal and hand-forearm dystonia, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the GNAL gene on chromosome 18p11. (3)
- References
-
- ICD10CM:G24.1
- OMIM:615073
- ORDO:329466
- Ontology
- Human Disease ( DOID:0090055 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations