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| Term | paroxysmal nonkinesigenic dyskinesia 2 | ID (Ontology) | DOID:0090047 (Human Disease) |
| Definition | A dystonia characterized by attacks of dystonic or choreathetotic movements precipitated by stress, fatigue, coffee or alcohol intake or menstruation that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 2q31. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ movement disease | |__dystonia____________________| paroxysmal nonkinesigenic dyskinesia 2 |
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| Is a |
autosomal dominant disease dystonia |
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External Crossreferences & Linkouts
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ICD10CM:G24.8 MESH:C567001 MIM:611147 ORDO:98810 |
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