Details of Disease | DrugMAP

General Information of Disease (ID: DISHTNFX)

Disease Name	Visceral neuropathy, familial, 2, autosomal recessive
Synonyms	VSCN2
Disease Hierarchy	DISKQ8R1: Visceral neuropathy, familial DISHTNFX: Visceral neuropathy, familial, 2, autosomal recessive
Disease Identifiers	MONDO ID MONDO_0030399 UMLS CUI C5561950 OMIM ID 619465 MedGen ID 1794160

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
ERBB2	TT6EO5L	Limited	Unknown	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ERBB2	OTOAUNCK	Limited	Unknown	[1]
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References

1	Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans. J Clin Invest. 2021 Mar 15;131(6):e145837. doi: 10.1172/JCI145837.