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: testicular non-seminomatous germ cell tumor (MONDO:0006447)
..Starting node ..testicular non-seminomatous germ cell cancer ()
Child Nodes:
........choriocarcinoma of testis ()
........testicular embryonal carcinoma ()
........testicular yolk sac tumor ()
Sister Nodes:
..testicular non-seminomatous germ cell cancer ()
..testicular trophoblastic tumor ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3403
Name:	testicular non-seminomatous germ cell cancer
Definition:	A classification of testicular cancers that arise in specialized sex cells called germ cells. Nonseminomas include embryonal carcinoma, teratoma, choriocarcinoma, and yolk sac tumor.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	malignant non-seminomatous germ cell cancer of testis; malignant non-seminomatous germ cell cancer of the testis; malignant non-seminomatous germ cell neoplasm of testis; malignant non-seminomatous germ cell neoplasm of the testis; malignant non-seminomatous germ cell tumor of testis; malignant non-
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal