Details of Disease | DrugMAP

General Information of Disease (ID: DISOCQGA)

Disease Name	Neurodevelopmental disorder with hyperkinetic movements and dyskinesia
Disease Hierarchy	DIS372XH: Neurodevelopmental disorder DISOCQGA: Neurodevelopmental disorder with hyperkinetic movements and dyskinesia
Disease Identifiers	MONDO ID MONDO_0859211 UMLS CUI C5562038 OMIM ID 619651 MedGen ID 1794248

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTT Molecule(s)

Gene Name	DTT ID	Evidence Level	Mode of Inheritance	REF
ADCY5	TTN64VU	Strong	Autosomal recessive	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ADCY5	OTF2WIT0	Strong	Autosomal recessive	[1]
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References

1	Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus. Neurol Genet. 2017 Sep 25;3(5):193. doi: 10.1212/NXG.0000000000000193. eCollection 2017 Oct.