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: nasal cavity carcinoma (MONDO:0003212)
..Starting node ..nasal cavity adenocarcinoma ()
Child Nodes:
Sister Nodes:
..carcinoma arising in nasal papillomatosis ()
..nasal cavity adenocarcinoma ()
..nasal cavity carcinoma in situ ()
..nasal cavity 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:	3211
Name:	nasal cavity adenocarcinoma
Definition:	A carcinoma that arises from glandular epithelial cells of the nasal cavity
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of nasal cavity; adenocarcinoma of the nasal cavity; nasal cavity adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal