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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

Disease Browser
Parent Node: Salivary Gland Diseases (D012466)
..Starting node ..Sialometaplasia, Necrotizing (D012797)
Child Nodes:
Sister Nodes:
..Aplasia of Lacrimal and Salivary Glands (C562407)
..Mikulicz' Disease (D008882)
..Parotid Diseases (D010305) 7
..Parotid Salivary Glands, Polycystic Disease of (C563951)
..Salivary Calculi (D020792) 2
..Salivary Gland Fistula (D012467)
..Salivary Gland Neoplasms (D012468) 6
..Sialadenitis (D012793) 6
..Sialometaplasia, Necrotizing (D012797)
..Sialorrhea (D012798)
..Submandibular Gland Diseases (D013364) 1
..Tunglang Savage Bellman syndrome (C536927)
..Xerostomia (D014987) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10220
Name:	Sialometaplasia, Necrotizing
Definition:	A benign, inflammatory, variably ulcerated, occasionally bilateral, self-healing lesion of the minor salivary glands that is often confused clinically and histologically with carcinoma.
Alternative IDs:
ParentIDs:	MESH:D012466
TreeNumbers:	C07.465.815.802
Synonyms:	Necrotizing Sialometaplasia \|Necrotizing Sialometaplasias \|Sialometaplasias, Necrotizing
Slim Mappings:	Mouth disease
Reference:	MedGen: D012797 MeSH: D012797 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants