Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the digestive system (HP:0025031)help
Parent Node:
expandAbnormality of the abdominal wall (HP:0004298)help
..Starting node
..expandPrune belly (HP:0004392)help
Term ID: 4392
Name: Prune belly
Synonym: Prune belly
Definition: A kind of congenital defect of the anterior abdominal wall in which the intestines are evident through the thin, lax, and protruding abdominal wall in affected infants.
Comments:
Reference: HP:0004392
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbdominal wall defect (HP:0010866) help
..expandAbnormal morphology of the abdominal musculature (HP:0010991) help
..expandAbnormal umbilicus morphology (HP:0001551) help
..expandExstrophy (HP:0100548) 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:0004392HP:0004392Prune belly0ALKBH8 CL E G H9180125189OMIM:618504Intellectual developmental disorder, autosomal recessive 71
HP:0004392HP:0004392Prune belly0CHRM3 CL E G H11311952OMIM:100100Prune belly syndrome.4
HP:0004392HP:0004392Prune belly0MYH11 CL E G H46297569OMIM:619351MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME 2; MMIHS2418
HP:0004392HP:0004392Prune belly0PIEZO1 CL E G H978028993OMIM:616843Lymphedema, hereditary, III36


Genes (4) :ALKBH8 CHRM3 MYH11 PIEZO1

Diseases (4) :OMIM:618504 OMIM:100100 OMIM:619351 OMIM:616843
 

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