MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: testicular cancer (MONDO:0005447)
..Starting node ..testicular lymphoma ()
Child Nodes:
Sister Nodes:
..malignant Sertoli-Leydig cell tumor ()
..malignant testicular germ cell tumor ()
..malignant testicular Leydig cell tumor ()
..malignant tumor of undescended testis ()
..rete testis adenocarcinoma ()
..seminal vesicle adenocarcinoma ()
..testicular gonadoblastoma (disease) ()
..testicular leukemia ()
..testicular lymphoma ()
..testis sarcoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1472
Name:	testicular lymphoma
Definition:	A lymphoma that arises from the testis and is not associated with lymphoma in another anatomic site.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	lymphoma of testis; lymphoma of the testis; malignant lymphoma of testis; primary testicular lymphoma; testicular lymphoma; TLYM
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal