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: glandular cell neoplasm (MONDO:0024276)
Parent Node: vulvar neoplasm (MONDO:0021049)
..Starting node ..vulvar glandular neoplasm ()
Child Nodes:
........Bartholin gland adenoma ()
........Bartholin gland adenomyoma ()
........minor vestibular glands adenoma ()
........vulvar adenocarcinoma ()
Sister Nodes:
..Bartholin gland neoplasm ()
..clitoris neoplasm ()
..germ cell tumor of the vulva ()
..paraurethral gland neoplasm ()
..polyp of vulva ()
..vulva cancer ()
..vulvar benign neoplasm ()
..vulvar glandular neoplasm ()
..vulvar granular cell tumor ()
..vulvar squamous neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2198
Name:	vulvar glandular neoplasm
Definition:	A benign or malignant neoplasm that arises from the vulva and is composed of glandular epithelial cells. Representative examples include adenoma of the minor vestibular glands, Bartholin gland adenoma, and Bartholin gland adenocarcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	mammalian vulva glandular cell neoplasm; vulvar glandular neoplasm; vulvar glandular tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal