MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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: lacrimal gland carcinoma (MONDO:0002463)
..Starting node ..lacrimal gland adenocarcinoma ()
Child Nodes:
........lacrimal gland adenoid cystic carcinoma ()
........lacrimal gland mucoepidermoid carcinoma ()
Sister Nodes:
..lacrimal gland adenocarcinoma ()
..lacrimal gland carcinoma ex pleomorphic adenoma ()
..lacrimal gland 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:	2475
Name:	lacrimal gland adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the lacrimal gland
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of lacrimal gland; adenocarcinoma of the lacrimal gland; lacrimal gland adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal