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: female reproductive organ cancer (MONDO:0001416)
..Starting node ..endometrioid adenocarcinoma ()
Child Nodes:
........cervical endometrioid adenocarcinoma ()
........endometrial endometrioid adenocarcinoma ()
........fallopian tube endometrioid adenocarcinoma ()
........ovarian endometrioid adenocarcinoma ()
Sister Nodes:
..adenocarcinofibroma ()
..adenosarcoma ()
..endometrioid adenocarcinoma ()
..fallopian tube cancer ()
..gestational choriocarcinoma ()
..ovarian cancer ()
..uterine cancer ()
..vaginal cancer ()
..vulva cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	5026
Name:	endometrioid adenocarcinoma
Definition:	An adenocarcinoma characterized by the presence of malignant glandular epithelial cells resembling endometrial cells. It can arise from the uterine body, ovary, fallopian tube, cervix, vagina, and uterine ligament.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	endometrioid adenocarcinoma; endometrioid carcinoma; endometrioid carcinoma of female reproductive system; endometrioid carcinoma of the female reproductive system; female reproductive endometrioid carcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal