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: benign male reproductive system neoplasm (MONDO:0000625)
Parent Node: neoplasm of testis (MONDO:0021348)
..Starting node ..benign neoplasm of testis ()
Child Nodes:
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:	21447
Name:	benign neoplasm of testis
Definition:	A benign neoplasm that involves the testis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign neoplasm of the testis; benign testicular neoplasm; benign testicular tumor; benign tumor of testis; benign tumor of the testis; testis benign neoplasm
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal