Human Phenotype Ontology 
Grandparent Node:
expandAbnormal rectum morphology (HP:0002034)help
Grandparent Node:
expandIntestinal fistula (HP:0100819)help
Grandparent Node:
expandUrogenital fistula (HP:0100589)help
Parent Node:
expandRectal fistula (HP:0100590)help
..Starting node
..expandRectovestibular fistula (HP:0025025)help
Term ID: 25025
Name: Rectovestibular fistula
Synonym: Vestibular fistula
Definition: A congenital malformation characterized by an abnormal connection (fistula) between the rectum and the vulval vestibule, at the lower aspect of the vaginal opening.
Comments:
Reference: HP:0025025
Genes and Diseases:
 
       Child Nodes:
........expandH-type rectovestibular fistula (HP:0025026) help

 Sister Nodes: 
..expandRectoperineal fistula (HP:0004792) help
..expandRectourethral fistula (HP:0025407) help
..expandRectovaginal fistula (HP:0000143) 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:0025025HP:0025025Rectovestibular fistula0PIGN CL E G H235568967ORPHA:280633Multiple congenital anomalies-hypotonia-seizures syndromeHP:0040283 - Occasional37
HP:0025025HP:0025026H-type rectovestibular fistula1 CL E G H


Genes (1) :PIGN

Diseases (1) :ORPHA:280633
 

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