Disease browser and phenotype portal

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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 ..Penile Diseases (D010409)
Child Nodes:
........Balanitis (D001446) 1
........Hypospadias (D007021) 17
........MORM syndrome (C536984)
........Penile Induration (D010411)
........Penile Neoplasms (D010412)
........Phimosis (D010688) 2
........Priapism (D011317) 1
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:	8772
Name:	Penile Diseases
Definition:	Pathological processes involving the PENIS or its component tissues.
Alternative IDs:
ParentIDs:	MESH:D005832
TreeNumbers:	C12.294.494
Synonyms:	Disease, Penile \|Disease, Penis \|Diseases, Penile \|Diseases, Penis \|Penile Disease \|Penis Disease \|Penis Diseases
Slim Mappings:	Urogenital disease (male)
Reference:	MedGen: D010409 MeSH: D010409 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants