OBO ID: DOID:0090055 |
Term Name: | dystonia 25 | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0090055 ) |
OTHER dystonia 25 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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