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: vulvar carcinoma (MONDO:0005215)
Parent Node: vulvar glandular neoplasm (MONDO:0002198)
..Starting node ..vulvar adenocarcinoma ()
Child Nodes:
........adenocarcinoma of skene gland origin ()
........Bartholin gland adenocarcinoma ()
........vulval Paget disease ()
........vulvar apocrine adenocarcinoma ()
........vulvar clear cell hidradenocarcinoma ()
........vulvar eccrine adenocarcinoma ()
........vulvar sebaceous carcinoma ()
Sister Nodes:
..Bartholin gland adenoma ()
..Bartholin gland adenomyoma ()
..minor vestibular glands adenoma ()
..vulvar adenocarcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	24336
Name:	vulvar adenocarcinoma
Definition:	An adenocarcinoma that arises from the vulva. Representative examples include Bartholin gland adenocarcinoma, eccrine adenocarcinoma, apocrine adenocarcinoma, and sebaceous carcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of the vulva; adenocarcinoma of vulva; mammalian vulva adenocarcinoma; vulva adenocarcinoma; vulvar adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal