Human Phenotype Ontology 
Grandparent Node:
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Abdominal symptom (HP:0011458)help
Grandparent Node:
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Pain (HP:0012531)help
Parent Node:
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Abdominal pain (HP:0002027)help
..Starting node
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Abdominal colic (HP:0011848)help
Term ID: 11848
Name: Abdominal colic
Synonym:
Definition: A type of abdominal pain that comes and goes in waves, most often starting and ending suddenly and being of severe intensity.
Comments:
Reference: HP:0011848
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEpisodic abdominal pain (HP:0002574) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011848HP:0011848Abdominal colic0ABCB4 CL E G H524445ORPHA:69663Low phospholipid-associated cholelithiasisHP:0040281 - Very frequent111
HP:0011848HP:0011848Abdominal colic0ALAD CL E G H210395OMIM:612740Porphyria, acute hepatic.62
HP:0011848HP:0011848Abdominal colic0APRT CL E G H353626ORPHA:976Adenine phosphoribosyltransferase deficiencyHP:0040283 - Occasional19
HP:0011848HP:0011848Abdominal colic0DGAT1 CL E G H86942843OMIM:615863Diarrhea 7, protein-losing Enteropathy type9
HP:0011848HP:0011848Abdominal colic0SI CL E G H647610856ORPHA:35122Congenital sucrase-isomaltase deficiencyHP:0040283 - Occasional98


Genes (5) :ABCB4 ALAD APRT DGAT1 SI

Diseases (5) :ORPHA:69663 OMIM:612740 ORPHA:976 OMIM:615863 ORPHA:35122
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.