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: malignant testicular germ cell tumor (MONDO:0003510)
Parent Node: seminoma (MONDO:0003001)
Parent Node: testicular pure germ cell tumor (MONDO:0002874)
..Starting node ..testicular seminoma ()
Child Nodes:
........cribriform variant testicular seminoma ()
........pseudoglandular variant testicular seminoma ()
........spermatocytic seminoma ()
........tubular variant testicular seminoma ()
Sister Nodes:
..testicular embryonal carcinoma ()
..testicular seminoma ()
..testicular trophoblastic tumor ()
..testicular yolk sac tumor ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3669
Name:	testicular seminoma
Definition:	A malignant germ cell tumor arising from the testis. It is believed that it is derived from the sexually undifferentiated embryonic gonad. Treatment with radiotherapy is highly successful when the tumor is diagnosed in localized stages, which represents the majority of presentations of seminoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	seminoma of testis; seminoma of the testis; seminoma testis; seminomatous germ cell tumor of testis; testicular seminoma; testicular seminoma (disease); testicular seminoma Pure; testicular seminomatous germ cell tumor; testis seminoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: PLOD1;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal