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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Genital Diseases, Male (D005832)
..Starting node ..Penis agenesis (C536649)
Child Nodes:
Sister Nodes:
..Epididymitis (D004823)
..Fournier Gangrene (D018934)
..Genital Neoplasms, Male (D005834) 34
..Hematocele (D006398)
..Hemospermia (D051516)
..Hennekam lymphangiectasia lymphedema syndrome (C537255)
..Herpes Genitalis (D006558)
..Infertility (D007246) 26
..Penile Diseases (D010409) 28
..Penis agenesis (C536649)
..Prostatic Diseases (D011469) 24
..Reproductive Tract Infections (D060737)
..Sexual Dysfunction, Physiological (D012735) 5
..Sexually Transmitted Diseases (D012749) 41
..Spermatic Cord Torsion (D013086)
..Spermatocele (D013088)
..Testicular Diseases (D013733) 28
..Testicular Hydrocele (D006848)
..Tuberculosis, Male Genital (D014389)
..Varicocele (D014646)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8775
Name:	Penis agenesis
Definition:
Alternative IDs:
ParentIDs:	MESH:D005832
TreeNumbers:	C12.294/C536649
Synonyms:	Agenesis of the penis \|Micropenis \|Penis agenesia
Slim Mappings:	Urogenital disease (male)
Reference:	MedGen: C536649 MeSH: C536649 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants