Details of Disease | DrugMAP

General Information of Disease (ID: DISENZKO)

Disease Name	Intestinal dysmotility syndrome
Disease Hierarchy	DISGPMUQ: Intestinal disorder DISENZKO: Intestinal dysmotility syndrome
Disease Identifiers	MONDO ID MONDO_0859289 UMLS CUI C5774219 OMIM ID 620045 MedGen ID 1823992

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
ANO1	TTOJI4S	Limited	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
ANO1	OTSREUNI	Limited	Autosomal recessive	[1]
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References

1	TMEM16A deficiency: a potentially fatal neonatal disease resulting from impaired chloride currents. J Med Genet. 2021 Apr;58(4):247-253. doi: 10.1136/jmedgenet-2020-106978. Epub 2020 Jun 2.