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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 ..Hemospermia (D051516)
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:	5066
Name:	Hemospermia
Definition:	Blood in the SEMEN, usually due to INFLAMMATION of the PROSTATE, the SEMINAL VESICLES, or both.
Alternative IDs:
ParentIDs:	MESH:D005832
TreeNumbers:	C12.294.293
Synonyms:	Hematospermia
Slim Mappings:	Urogenital disease (male)
Reference:	MedGen: D051516 MeSH: D051516 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants