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 non-seminomatous germ cell tumor ()
Child Nodes:
........testicular non-seminomatous germ cell cancer ()
........testicular trophoblastic 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:	6447
Name:	testicular non-seminomatous germ cell tumor
Definition:	A testicular germ cell tumor characterized by the absence of a seminomatous component. It includes embryonal carcinoma, yolk sac tumor, choriocarcinoma, teratoma, and mixed forms.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	non-dysgerminomatous germ cell tumor of testis; non-seminomatous germ cell tumor of testis; testicular germ cell tumor non-seminomatous; testicular non seminomatous germ cell tumor; testicular non-dysgerminomatous germ cell tumor; testicular non-seminomatous germ cell tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: TRIM32;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal