Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of male external genitalia (HP:0000032)help
Parent Node:
expandAbnormal penis morphology (HP:0000036)help
..Starting node
..expandAbnormality of corpus cavernosum (HP:0100623)help
Term ID: 100623
Name: Abnormality of corpus cavernosum
Synonym:
Definition:
Comments:
Reference: HP:0100623
Genes and Diseases:
 
       Child Nodes:
........expandCorpus cavernosum sclerosis (HP:0100624) help

 Sister Nodes: 
..expandAbnormal preputium morphology (HP:0100587) help
..expandAbsent penis (HP:0030261) help
..expandBifid penis (HP:0100599) help
..expandChordee (HP:0000041) help
..expandDisplacement of the urethral meatus (HP:0100627) help
..expandErectile dysfunction (HP:0100639) help
..expandHypoplasia of penis (HP:0008736) help
..expandLong penis (HP:0000040) help
..expandNarrow penis (HP:0030262) help
..expandNeoplasm of the penis (HP:0100850) help
..expandPartial development of the penile shaft (HP:0008708) help
..expandPenile freckling (HP:0031447) help
..expandPenoscrotal transposition (HP:0100600) help
..expandTorsion of the penis (HP:0030263) help
..expandWebbed penis (HP:0030264) 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:0100623HP:0100623Abnormality of corpus cavernosum0 CL E G H
HP:0100623HP:0100624Corpus cavernosum sclerosis1 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.