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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 ..Xerostomia (D014987)
Child Nodes:
........Sjogren's Syndrome (D012859) 1
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:	11832
Name:	Xerostomia
Definition:	Decreased salivary flow.
Alternative IDs:
ParentIDs:	MESH:D012466
TreeNumbers:	C07.465.815.929
Synonyms:	Asialia \|Asialias \|Dryness, Mouth \|Hyposalivation \|Hyposalivations \|Mouth Dryness \|Xerostomias
Slim Mappings:	Mouth disease
Reference:	MedGen: D014987 MeSH: D014987 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants