Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of male external genitalia (HP:0000032)help
Grandparent Node:
expandAbnormality of the lower urinary tract (HP:0010936)help
Parent Node:
expandAbnormality of the urethra (HP:0000795)help
..Starting node
..expandCongenital megalourethra (HP:0030723)help
Term ID: 30723
Name: Congenital megalourethra
Synonym:
Definition: Dilation and elongation of the penile urethra associated with absence or hypoplasia of the corpora spongiosa and cavernosa.
Comments:
Reference: HP:0030723
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..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
..expandUrethritis (HP:0500006) 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:0030723HP:0030723Congenital megalourethra0 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.