Human Phenotype Ontology 
Grandparent Node:
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Abnormality of male external genitalia (HP:0000032)help
Grandparent Node:
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Abnormality of the lower urinary tract (HP:0010936)help
Parent Node:
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Abnormality of the urethra (HP:0000795)help
..Starting node
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Urethritis (HP:0500006)help
Term ID: 500006
Name: Urethritis
Synonym:
Definition: Inflammation of the urethra.
Comments:
Reference: HP:0500006
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCongenital megalourethra (HP:0030723) help
..expandDisplacement of the urethral meatus (HP:0100627) help
..expandDistal urethral duplication (HP:0008706) help
..expandNeoplasm of the urethra (HP:0100517) help
..expandPatulous urethra (HP:0025417) help
..expandUrethral atresia (HP:0000068) help
..expandUrethral diverticulum (HP:0008722) help
..expandUrethral fistula (HP:0010480) help
..expandUrethral obstruction (HP:0000796) help
..expandUrethrocele (HP:0100821) help
..expandUrogenital sinus anomaly (HP:0100779) 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:0500006HP:0500006Urethritis0 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.