Details of Disease | DrugMAP

General Information of Disease (ID: DISJTXWX)

Disease Name	Neurodevelopmental disorder with or without variable movement or behavioral abnormalities
Disease Hierarchy	DIS372XH: Neurodevelopmental disorder DISJTXWX: Neurodevelopmental disorder with or without variable movement or behavioral abnormalities
Disease Identifiers	MONDO ID MONDO_0859225 UMLS CUI C5676908 OMIM ID 619725 MedGen ID 1802087

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
KCNN2	TT2T5M0	Strong	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
KCNN2	OTQVTMK5	Strong	Autosomal dominant	[1]
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References

1	The frissonnant mutant mouse, a model of dopamino-sensitive, inherited motor syndrome. Neurobiol Dis. 2001 Jun;8(3):447-58. doi: 10.1006/nbdi.2001.0393.