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Myoclonic Epilepsy, Juvenile

Disease ID: disease_node_10189

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DbxrefGARD:6808, MESH:D020190, MIM:254770, NCI:C84796, ORDO:307, ORDO:862, SNOMEDCT_US_2023_03_01:6204001, UMLS_CUI:C0270853
SubclassofDOID_0050705
Data SourceDOID, MESH
SynonymsJanz syndrome
Mesh IdD020190
Mesh LabelMyoclonic Epilepsy, Juvenile
Mesh SubclassofD004831
Doid Labeljuvenile myoclonic epilepsy
Doid DescriptionA adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years. Xref MGI. OMIM mapping confirmed by DO. [SN].
Has PhenotypeHP_0001336
Existence Starts DuringHP_0011462
Disease Node Iddisease_node_10189
Doid IdDOID_4890
LabelMyoclonic Epilepsy, Juvenile
Doid Alternate IdsDOID_0050326