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: maxillary sinus carcinoma (MONDO:0001748)
..Starting node ..maxillary sinus adenocarcinoma ()
Child Nodes:
Sister Nodes:
..maxillary sinus adenocarcinoma ()
..maxillary sinus adenoid cystic carcinoma ()
..maxillary 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:	4328
Name:	maxillary sinus adenocarcinoma
Definition:	An adenocarcinoma that arises from the maxillary sinus. It is classified as intestinal-type or non-intestinal-type adenocarcinoma. Nasal obstruction and epistaxis are the presenting signs.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of maxillary sinus; adenocarcinoma of the maxillary sinus; maxillary sinus adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal