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DOID:0090037 - torsion dystonia 13
Disease Ontology Definition:A dystonia characterized by autosomal dominant inheritance of focal or segmental dystonia with cranial, cervical, or upper limb involvement that has_material_basis_in variation in the chromosome region 1p36.32-p36.13.
Synonyms:
Xenbase Genes :
MONDO:0011886 - torsion dystonia 13 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
dystonia (is_a)