association	dataset	threshold value	standardized value
all	HPO Gene-Disease Associations	1.0	null
phenotypic abnormality	HPO Gene-Disease Associations	1.0	null
mechanical ileus	HPO Gene-Disease Associations	1.0	null
meconium ileus	HPO Gene-Disease Associations	1.0	null
abnormality of the abdomen	HPO Gene-Disease Associations	1.0	null
CYSTIC FIBROSIS, MODIFIER OF, 1	CTD Gene-Disease Associations	1.0	2.88009
intestinal obstruction	HPO Gene-Disease Associations	1.0	null
gastrointestinal obstruction	HPO Gene-Disease Associations	1.0	null
{meconium ileus in cystic fibrosis, susceptibility to}	OMIM Gene-Disease Associations	1.0	null
abnormality of the abdominal organs	HPO Gene-Disease Associations	1.0	null
morphological abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
gastrointestinal dysmotility	HPO Gene-Disease Associations	1.0	null
abnormality of the intestine	HPO Gene-Disease Associations	1.0	null
abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null
ileus	HPO Gene-Disease Associations	1.0	null
functional abnormality of the gastrointestinal tract	HPO Gene-Disease Associations	1.0	null