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: adenocarcinoma (MONDO:0004970)
Parent Node: prostate carcinoma (MONDO:0005159)
..Starting node ..prostate adenocarcinoma ()
Child Nodes:
........prostate adenoid cystic carcinoma ()
........prostatic acinar adenocarcinoma ()
Sister Nodes:
..familial prostate carcinoma ()
..grade III prostatic intraepithelial neoplasia ()
..hormone-resistant prostate carcinoma ()
..metastatic prostate carcinoma ()
..primary prostate urothelial carcinoma ()
..prostate adenocarcinoma ()
..prostate carcinoma in situ ()
..prostate small cell carcinoma ()
..prostate squamous cell carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5082
Name:	prostate adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the prostate gland
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of prostate; adenocarcinoma of the prostate; prad; prostate adenocarcinoma; prostate gland adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal