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: mixed germ cell tumor (MONDO:0015864)
..Starting node ..mixed testicular germ cell cancer ()
Child Nodes:
........childhood testicular mixed germ cell tumor ()
Sister Nodes:
..mixed extragonadal germ cell cancer ()
..mixed germ cell tumor of vulva ()
..mixed teratoma and seminoma ()
..mixed testicular germ cell cancer ()
..ovarian mixed germ cell neoplasm ()
..teratocarcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3120
Name:	mixed testicular germ cell cancer
Definition:	A malignant germ cell tumor that arises from the testis and is characterized by the presence of more than one histologic component. Representative examples include mixed choriocarcinoma and embryonal carcinoma, mixed embryonal carcinoma and seminoma, and mixed yolk sac tumor and teratoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	mixed germ cell neoplasm of testis; mixed germ cell neoplasm of the testis; mixed germ cell tumor; mixed germ cell tumor of testis; mixed germ cell tumor of the testis; mixed testicular germ cell tumor; testicular germ cell tumor (mixed); testicular mixed germ cell neoplasm; testicular mixed germ ce
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
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