Human Phenotype Ontology 
Grandparent Node:
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Abnormal vagina morphology (HP:0000142)help
Grandparent Node:
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Urogenital fistula (HP:0100589)help
Parent Node:
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Urethral fistula (HP:0010480)help
Parent Node:
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Vaginal fistula (HP:0004320)help
..Starting node
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Urethrovaginal fistula (HP:0008716)help
Term ID: 8716
Name: Urethrovaginal fistula
Synonym: Urethrovaginal fistulae
Definition: The presence of a fistula between the vagina and the urethra.
Comments:
Reference: HP:0008716
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandRectovaginal fistula (HP:0000143) help
..expandVesicovaginal fistula (HP:0001586) 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:0008716HP:0008716Urethrovaginal fistula0DYNC2H1 CL E G H796592962ORPHA:93271Short rib-polydactyly syndrome, Verma-Naumoff typeHP:0040282 - Frequent304
HP:0008716HP:0008716Urethrovaginal fistula0DYNC2I1 CL E G H5511221862ORPHA:93271Short rib-polydactyly syndrome, Verma-Naumoff typeHP:0040282 - Frequent
HP:0008716HP:0008716Urethrovaginal fistula0DYNC2I2 CL E G H8989128296ORPHA:93271Short rib-polydactyly syndrome, Verma-Naumoff typeHP:0040282 - Frequent
HP:0008716HP:0008716Urethrovaginal fistula0IFT80 CL E G H5756029262ORPHA:93271Short rib-polydactyly syndrome, Verma-Naumoff typeHP:0040282 - Frequent65
HP:0008716HP:0008716Urethrovaginal fistula0UBR1 CL E G H19713116808OMIM:243800Johanson-Blizzard syndrome.25
HP:0008716HP:0008716Urethrovaginal fistula0WDR35 CL E G H5753929250ORPHA:93271Short rib-polydactyly syndrome, Verma-Naumoff typeHP:0040282 - Frequent136


Genes (6) :DYNC2H1 DYNC2I1 DYNC2I2 IFT80 UBR1 WDR35

Diseases (2) :ORPHA:93271 OMIM:243800
 

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