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 neoplasm (MONDO:0021079)
Parent Node: neoplasm of testis (MONDO:0021348)
..Starting node ..childhood testicular neoplasm ()
Child Nodes:
........childhood testicular germ cell tumor ()
Sister Nodes:
..benign neoplasm of testis ()
..childhood testicular neoplasm ()
..rete testis neoplasm ()
..seminal vesicle tumor ()
..testicular Brenner tumor ()
..testicular cancer ()
..testicular germ cell tumor ()
..testicular sex cord-stromal neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	37250
Name:	childhood testicular neoplasm
Definition:	A neoplasm that arises from the testis during childhood.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	childhood neoplasm of testis; childhood neoplasm of the testis; childhood testicular neoplasm; neoplasm of testis of childhood; pediatric neoplasm of testis; pediatric neoplasm of testis; pediatric neoplasm of the testis; pediatric testicular neoplasm; testicular tumor, childhood
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal