DisGeNET - a database of gene-disease associations

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Gene

Disease

Variant

Source

Semantic type

Disease Class

Type

HPO Term

DO Class

CUI	Disease	Type	Disease Class	Semantic type	DO Class	HPO Term	Num. genes	Num. SNPs
C4023588	Abnormality of the gastrointestinal tract	phenotype	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases	Anatomical Abnormality		Abnormality of the digestive system	14	1