Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the digestive system (HP:0025031)help
Parent Node:
expandAbnormal abdomen morphology (HP:0001438)help
..Starting node
..expandPelvic organ prolapse (HP:0031607)help
Term ID: 31607
Name: Pelvic organ prolapse
Synonym:
Definition: Weakness in the supporting structures of the pelvic floor allowing the pelvic viscera to descend or one or more of the pelvic organs drop from their normal position.
Comments:
Reference: HP:0031607
Genes and Diseases:
 
       Child Nodes:
........expandCystocele (HP:0100645) help

 Sister Nodes: 
..expandAbdominal aseptic abscess (HP:0025181) help
..expandAbdominal mass (HP:0031500) help
..expandAscites (HP:0001541) help
..expandDuplication of internal organs (HP:0005217) help
..expandPelvic mass (HP:0031501) help
..expandVisceromegaly (HP:0003271) 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:0031607HP:0031607Pelvic organ prolapse0COL3A1 CL E G H12812201OMIM:130050Ehlers-Danlos syndrome, Vascular type749
HP:0031607HP:0031607Pelvic organ prolapse0COL3A1 CL E G H12812201ORPHA:286Vascular Ehlers-Danlos syndrome749
HP:0031607HP:0031607Pelvic organ prolapse0SMAD3 CL E G H40886769OMIM:613795LOEYS-DIETZ SYNDROME 3; LDS3260
HP:0031607HP:0100645Cystocele1COL3A1 CL E G H12812201OMIM:130050Ehlers-Danlos syndrome, Vascular type.749
HP:0031607HP:0100645Cystocele1COL3A1 CL E G H12812201ORPHA:286Vascular Ehlers-Danlos syndromeHP:0040283 - Occasional749
HP:0031607HP:0100645Cystocele1SMAD3 CL E G H40886769OMIM:613795LOEYS-DIETZ SYNDROME 3; LDS3260


Genes (2) :COL3A1 SMAD3

Diseases (3) :OMIM:130050 ORPHA:286 OMIM:613795
 

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