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: male reproductive system neoplasm (MONDO:0024582)
Parent Node: reproductive system cancer (MONDO:0002149)
..Starting node ..male reproductive organ cancer ()
Child Nodes:
........carcinoma of Cowper glands ()
........epididymis cancer ()
........penile cancer ()
........prostate cancer ()
........scrotum cancer ()
........spermatic cord cancer ()
........testicular cancer ()
Sister Nodes:
..Buschke Lowenstein tumor ()
..female reproductive organ cancer ()
..gonadoblastoma ()
..male reproductive organ cancer ()
..malignant Leydig cell tumor ()
..malignant Sertoli cell tumor ()
..prepuce cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5836
Name:	male reproductive organ cancer
Definition:	A primary or metastatic malignant neoplasm involving the male reproductive system. Representative examples include prostate carcinoma, penile carcinoma, testicular seminoma, and testicular embryonal carcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cancer of male reproductive organ; male genital cancer; male genital neoplasm; Male reprod. system cancer, NOS; male reproductive organ cancer; Male reproductive system cancer, NOS; male reproductive system neoplasm; malignant male reproductive organ neoplasm; malignant Male reproductive system neop
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal