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 germ cell tumor (MONDO:0006290)
Parent Node: testicular cancer (MONDO:0005447)
Parent Node: testicular germ cell tumor (MONDO:0010108)
..Starting node ..malignant testicular germ cell tumor ()
Child Nodes:
........malignant teratoma of testis ()
........mixed testicular germ cell cancer ()
........testicular non-seminomatous germ cell cancer ()
........testicular seminoma ()
........testis polyembryoma ()
........testis refractory cancer ()
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:	3510
Name:	malignant testicular germ cell tumor
Definition:	A malignant tumor predominantly affecting young men and often associated with cryptorchidism. Seminoma is the most frequently seen malignant testicular germ cell tumor, followed by embryonal carcinoma and yolk sac tumor.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	malignant germ cell neoplasm of testis; malignant germ cell neoplasm of the testis; malignant germ cell tumor of testis; malignant germ cell tumor of the testis; malignant testicular germ cell neoplasm; malignant testicular germ cell tumor; testicular ca. (no germ/tropho.); testicular cancer; testic
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal