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: digestive system neoplasm (MONDO:0021223)
Parent Node: head and neck neoplasm (MONDO:0005586)
Parent Node: salivary gland disease (MONDO:0001142)
..Starting node ..tumor of salivary gland ()
Child Nodes:
........benign neoplasm of salivary gland ()
........neoplasm of major salivary gland ()
........neoplasm of minor salivary gland ()
........salivary gland cancer ()
Sister Nodes:
..benign lymphoepithelial lesion of salivary gland ()
..mucocele of salivary gland ()
..necrotizing sialometaplasia ()
..parotid disease ()
..sialadenitis ()
..sialolithiasis ()
..Sjogren syndrome ()
..submandibular gland disease ()
..tumor of salivary gland ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21357
Name:	tumor of salivary gland
Definition:	A neoplasm (disease) that involves the saliva-secreting gland.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	neoplasm of saliva-secreting gland; neoplasm of salivary gland; neoplasm of the salivary gland; saliva-secreting gland neoplasm; saliva-secreting gland neoplasm (disease); saliva-secreting gland tumor; salivary gland neoplasm; salivary gland tumor; tumor of saliva-secreting gland; tumor of the saliv
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal