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Disease Ontology Browser
torsion dystonia with onset in infancy (DOID:0090058)
Alliance: disease page
Alt IDs: OMIM:602554, ICD10CM:G24.1, MESH:C536969, ORDO:256
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory