MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation 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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: infectious disease (MONDO:0005550)
Parent Node: inflammatory disease (MONDO:0021166)
Parent Node: male reproductive system disease (MONDO:0003150)
..Starting node ..epididymitis (disease) ()
Child Nodes:
........epididymo-orchitis ()
........tuberculous epididymitis ()
Sister Nodes:
..benign male reproductive system neoplasm ()
..cryptorchidism (disease) ()
..epididymitis (disease) ()
..fournier gangrene ()
..genital herpes ()
..hematocele of tunica vaginalis testis ()
..hydrocele ()
..male genital organ stricture ()
..male genital organ vascular disease ()
..male infertility ()
..male reproductive system neoplasm ()
..non-syndromic urogenital tract malformation of male ()
..penile disease ()
..prostate disease ()
..scrotal disease ()
..spermatocele ()
..teratozoospermia ()
..testicular disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4779
Name:	epididymitis (disease)
Definition:	Inflammation of the epididymis. Its clinical features include enlarged epididymis, a swollen scrotum; pain; pyuria; and fever. It is usually related to infections in the urinary tract, which likely spread to the epididymis through either the vas deferens or the lymphatics of the spermatic cord.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	epididymal; epididymis; epididymitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
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