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: autoimmune disease of exocrine system (MONDO:0000586)
Parent Node: salivary gland disease (MONDO:0001142)
..Starting node ..benign lymphoepithelial lesion of salivary gland ()
Child Nodes:
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:	1598
Name:	benign lymphoepithelial lesion of salivary gland
Definition:	A benign lesion that involves the salivary glands, usually the parotid gland. It affects females more often than males and it may be a manifestation of autoimmune diseases such as Sjogren syndrome. There is an increased incidence of benign lymphoepithelial lesions in HIV-positive patients. It is characterized by the presence of a marked lymphocytic infiltrate and epi-myoepithelial islands in the affected salivary gland. Patients usually present with firm and painless swelling of the affected salivary gland. There is an increased risk for development of lymphoma.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	benign lymphoepithelial lesion of salivary gland; benign lymphoepithelial lesion of the salivary gland; benign salivary gland lymphoepithelial lesion; Godwin tumor
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
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