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: submandibular gland cancer (MONDO:0004724)
..Starting node ..submandibular gland adenocarcinoma ()
Child Nodes:
Sister Nodes:
..mucoepidermoid carcinoma of submandibular gland ()
..submandibular gland adenocarcinoma ()
..submandibular gland adenoid cystic carcinoma ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6435
Name:	submandibular gland adenocarcinoma
Definition:	An adenocarcinoma that arises from the submandibular gland. Representative examples include polymorphic low-grade adenocarcinoma and acinic cell carcinoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	adenocarcinoma of submandibular gland; adenocarcinoma of the submandibular gland; submandibular gland adenocarcinoma
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal