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DOID:0090058 - torsion dystonia with onset in infancy
Disease Ontology 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.
Synonyms:
Xenbase Genes :
MONDO:0011249 - torsion dystonia with onset in infancy |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee