OBO ID: DOID:0090037 |
Term Name: | torsion dystonia 13 | Search Ontology: | |
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Definition: | A dystonia that is characterized by focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 1p36.32-p36.13. (2) | ||
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Ontology: | Human Disease ( DOID:0090037 ) |
OTHER torsion dystonia 13 PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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