Human Phenotype Ontology 
Grandparent Node:
expandAbnormal intestine morphology (HP:0002242)help
Parent Node:
expandAbnormality of the small intestine (HP:0002244)help
..Starting node
..expandAgenesis of the small intestine (HP:0012739)help
Term ID: 12739
Name: Agenesis of the small intestine
Synonym: Small bowel agenesis; Undeveloped small intestine
Definition: Failure to develop of the small intestine.
Comments:
Reference: HP:0012739
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal duodenum morphology (HP:0002246) help
..expandAbnormal ileum morphology (HP:0001549) help
..expandAbnormal jejunum morphology (HP:0005265) help
..expandAbnormal small intestinal mucosa morphology (HP:0025129) help
..expandAbnormality of small intestinal villus morphology (HP:0011472) help
..expandCeliac disease (HP:0002608) help
..expandCongenital shortened small intestine (HP:0030889) help
..expandFat malabsorption (HP:0002630) help
..expandHypoplasia of the small intestine (HP:0004790) help
..expandMalrotation of small bowel (HP:0004794) help
..expandProtein-losing enteropathy (HP:0002243) help
..expandSmall bowel diverticula (HP:0002256) help
..expandSmall intestinal bleeding (HP:0012849) help
..expandSmall intestinal dysmotility (HP:0012850) help
..expandSmall intestinal stenosis (HP:0012848) 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:0012739HP:0012739Agenesis of the small intestine0 CL E G H


Genes (0) :

Diseases (0) :
 

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