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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: Cysts (D003560)
Parent Node: Genital Diseases, Male (D005832)
..Starting node ..Spermatocele (D013088)
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:	10437
Name:	Spermatocele
Definition:	A cystic dilation of the EPIDIDYMIS, usually in the head portion (caput epididymis). The cyst fluid contains dead SPERMATOZOA and can be easily differentiated from TESTICULAR HYDROCELE and other testicular lesions.
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D005832
TreeNumbers:	C12.294.731 \|C23.300.306.750
Synonyms:	Cyst, Epididymal \|Cysts, Epididymal \|Epididymal Cyst \|Epididymal Cysts \|Spermatoceles
Slim Mappings:	Pathology (anatomical condition)\|Urogenital disease (male)
Reference:	MedGen: D013088 MeSH: D013088 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants