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: neoplasm of testis (MONDO:0021348)
..Starting node ..seminal vesicle tumor ()
Child Nodes:
........seminal vesicle adenocarcinoma ()
........seminal vesicle cystadenoma ()
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:	2790
Name:	seminal vesicle tumor
Definition:	A benign or malignant neoplasm that affects the seminal vesicle. Representative examples include cystadenoma and adenocarcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	neoplasm of seminal vesicle; seminal vesicle neoplasm; seminal vesicle neoplasm (disease); seminal vesicle tumor; tumor of seminal vesicle
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: CYP2A6; CYP2C9; F9; VKORC1;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal