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: testicular germ cell tumor (MONDO:0010108)
..Starting node ..testicular pure germ cell tumor ()
Child Nodes:
........testicular embryonal carcinoma ()
........testicular seminoma ()
........testicular trophoblastic tumor ()
........testicular yolk sac tumor ()
Sister Nodes:
..childhood testicular germ cell tumor ()
..malignant testicular germ cell tumor ()
..testicular non-seminomatous germ cell tumor ()
..testicular pure germ cell tumor ()
..testicular teratoma ()
..TGCT1 ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2874
Name:	testicular pure germ cell tumor
Definition:	A germ cell tumor that arises from the testis and is characterized by the presence of one histologic component. This category includes seminoma, teratoma, embryonal carcinoma, yolk sac tumor, and trophoblastic tumor.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	testicular Pure germ cell tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
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