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: Brenner tumor (MONDO:0024235)
Parent Node: neoplasm of testis (MONDO:0021348)
..Starting node ..testicular Brenner tumor ()
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:	3118
Name:	testicular Brenner tumor
Definition:	An uncommon usually benign neoplasm that arises from the testis. It is characterized by the presence of cysts lined by transitional cells and solid nests of transitional cells in a spindle cell stroma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	testes, rudimentary Brenner tumor; testis Brenner tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal