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: vaginal carcinoma (MONDO:0015867)
Parent Node: vaginal glandular neoplasm (MONDO:0001704)
..Starting node ..vaginal adenocarcinoma ()
Child Nodes:
........vaginal adenoid cystic carcinoma ()
Sister Nodes:
..vaginal adenocarcinoma ()
..vaginal adenoma ()
..vaginal mullerian papilloma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	20653
Name:	vaginal adenocarcinoma
Definition:	An adenocarcinoma arising from the vagina. Morphologic variants include the clear cell, endometrioid, mesonephric, and mucinous adenocarcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of the vagina; adenocarcinoma of vagina; vagina adenocarcinoma; vaginal adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal