Human Phenotype Ontology 
Grandparent Node:
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Abnormality of male external genitalia (HP:0000032)help
Parent Node:
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Abnormal penis morphology (HP:0000036)help
Parent Node:
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Abnormality of the scrotum (HP:0000045)help
..Starting node
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Penoscrotal transposition (HP:0100600)help
Term ID: 100600
Name: Penoscrotal transposition
Synonym: Prepenile scrotum
Definition: A partial or complete positional exchange between the penis and the scrotum, with positioning of the scrotum superior to the penis.
Comments:
Reference: HP:0100600
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal scrotal rugation (HP:0012856) help
..expandAbsent scrotum (HP:0008707) help
..expandAccessory scrotum (HP:0030274) help
..expandBifid scrotum (HP:0000048) help
..expandEctopic scrotum (HP:0030275) help
..expandNeoplasm of the scrotum (HP:0100849) help
..expandobsolete Small scrotum (HP:0030276) help
..expandProminent scrotal raphe (HP:0003246) help
..expandScrotal hyperpigmentation (HP:0012855) help
..expandScrotal pain (HP:0030155) help
..expandShawl scrotum (HP:0000049) help
..expandSmall scrotum (HP:0000046) help
..expandVaginal hematocele (HP:0100674) help
..expandVaginal hydrocele (HP:0100673) help
..expandVaginal lymphocele (HP:0100676) help
..expandVaginal pyocele (HP:0100675) help
..expandVaricocele (HP:0012871) 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:0100600HP:0100600Penoscrotal transposition0 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.