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
Ontology
Human Disease   ( DOID:0090055 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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