Details of Disease | DrugMAP

General Information of Disease (ID: DISULBHG)

Disease Name	Chronic enteropathy associated with SLCO2A1 gene
Synonyms	CEAS
Disease Hierarchy	DISGPMUQ: Intestinal disorder DISULBHG: Chronic enteropathy associated with SLCO2A1 gene
Disease Identifiers	MONDO ID MONDO_0018766 UMLS CUI C5568838 MedGen ID 1800261 Orphanet ID 468641 SNOMED CT ID 1187194006

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLCO2A1	DT021JD	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
SLCO2A1	OT3062CA	Supportive	Autosomal recessive	[1]
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References

1	A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter. PLoS Genet. 2015 Nov 5;11(11):e1005581. doi: 10.1371/journal.pgen.1005581. eCollection 2015 Nov.