Details of Disease | DrugMAP

General Information of Disease (ID: DIS38WS1)

Disease Name	Familial gastric type 1 neuroendocrine tumor
Synonyms	familial type 1 gNET; hereditary type 1 gNET
Definition	Editor note: align gNET typology. See PMID:9041691 https://jamanetwork.com/journals/jamasurgery/fullarticle/390859
Disease Hierarchy	DIS0DAK3: Gastric neuroendocrine tumor, well differentiated, low or intermediate grade DIS38WS1: Familial gastric type 1 neuroendocrine tumor
Disease Identifiers	MONDO ID MONDO_0018742 UMLS CUI C5681095 MedGen ID 1826112 Orphanet ID 464756 SNOMED CT ID 1264340007

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
ATP4A	TTF1QVM	Supportive	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
ATP4A	OTOEGQOL	Supportive	Autosomal recessive	[1]
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References

1	Exome sequencing identifies ATP4A gene as responsible of an atypical familial type I gastric neuroendocrine tumour. Hum Mol Genet. 2015 May 15;24(10):2914-22. doi: 10.1093/hmg/ddv054. Epub 2015 Feb 11.