Search Ontology:
Human Disease

myoclonic dystonia 15

Term ID
DOID:0090035
Synonyms
Definition
A myoclonic dystonia that is characterized by jerky movements of the upper limbs, hands, and axial muscles, and has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 18p11. (2)
References
Ontology
Human Disease   ( DOID:0090035 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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