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: childhood gonadal germ cell tumor (MONDO:0020577)
Parent Node: childhood testicular neoplasm (MONDO:0037250)
Parent Node: testicular germ cell tumor (MONDO:0010108)
..Starting node ..childhood testicular germ cell tumor ()
Child Nodes:
........childhood embryonal testis carcinoma ()
........childhood testicular choriocarcinoma ()
........childhood testicular mixed germ cell 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:	3758
Name:	childhood testicular germ cell tumor
Definition:	A germ cell tumor that arises from the testis during childhood.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	childhood testicular germ cell neoplasm; childhood testicular germ cell tumor; pediatric testicular germ cell neoplasm; pediatric testicular germ cell tumor; pediatric testicular germ cell tumor; testicular germ cell tumor; testicular germ cell tumor of childhood
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal