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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: Parotid Diseases (D010305)
Parent Node: Salivary Gland Neoplasms (D012468)
..Starting node ..Parotid Neoplasms (D010307)
Child Nodes:
........Xanthogranulomatous sialadenitis (C536763)
Sister Nodes:
..Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia (C566352)
..Parotid Neoplasms (D010307) 1
..Salivary Gland Adenoma, Pleomorphic (C563250)
..Sublingual Gland Neoplasms (D013362)
..Submandibular Gland Neoplasms (D013365)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8680
Name:	Parotid Neoplasms
Definition:	Tumors or cancer of the PAROTID GLAND.
Alternative IDs:
ParentIDs:	MESH:D010305\|MESH:D012468
TreeNumbers:	C04.588.443.591.824.695 \|C07.465.565.824.695 \|C07.465.815.470.770 \|C07.465.815.718.589
Synonyms:	Cancer of Parotid \|Cancer of the Parotid \|Cancer, Parotid \|Cancers, Parotid \|Neoplasm, Parotid \|Neoplasms, Parotid \|Parotid Cancer \|Parotid Cancers \|Parotid Neoplasm
Slim Mappings:	Cancer\|Mouth disease
Reference:	MedGen: D010307 MeSH: D010307 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants