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| Term | torsion dystonia with onset in infancy | ID (Ontology) | DOID:0090058 (Human Disease) |
| Definition | A generalized dystonia that is characterized by autosomal dominant inheritance of generalized dystonia with severe involvement of the legs, mild involvement of the face and arms, and onset in infancy. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
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__ dystonia | |__generalized dystonia________| torsion dystonia with onset in infancy |
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| Parents/Children View Depth |
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Relationships
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| Is a |
autosomal dominant disease generalized dystonia |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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ICD10CM:G24.1 MESH:C536969 MIM:602554 ORDO:256 |
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