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DOID:0090041 - torsion dystonia 4
Disease Ontology Definition:A dystonia that is characterized by progressive laryngeal and cervical dystonia (onset in the second to third decade of life) followed by involvement of other muscles, such as the neck or limbs that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the tubulin beta 4A class IVa (TUBB4A) gene on chromosome 19p13.
Synonyms:
Xenbase Genes
:
tubb4a
| MONDO:0007493 - torsion dystonia 4 |
| MIM:128101 - DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
dystonia (is_a)