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 teratoma (MONDO:0003514)
Parent Node: malignant testicular germ cell tumor (MONDO:0003510)
..Starting node ..malignant teratoma of testis ()
Child Nodes:
Sister Nodes:
..malignant teratoma of testis ()
..mixed testicular germ cell cancer ()
..testicular non-seminomatous germ cell cancer ()
..testicular seminoma ()
..testis polyembryoma ()
..testis refractory cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21282
Name:	malignant teratoma of testis
Definition:	A malignant teratoma that involves the testis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	immature teratoma of testis; immature teratoma of the testis; immature testicular teratoma; malignant teratoma of the testis; malignant testicular teratoma; testicular immature teratoma; testicular malignant teratoma; testis malignant teratoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal