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: ethmoid sinus cancer (MONDO:0001763)
..Starting node ..ethmoid sinus adenocarcinoma ()
Child Nodes:
Sister Nodes:
..ethmoid sinus adenocarcinoma ()
..ethmoid sinus adenoid cystic carcinoma ()
..ethmoid sinus 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:	2418
Name:	ethmoid sinus adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the epithelial cell
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of ethmoid sinus; adenocarcinoma of the ethmoid sinus
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal