OBO ID: DOID:0090055
Term Name: dystonia 25 Search Ontology:
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 dystonia 25 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNAL Dystonia 25 615073
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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