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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: Sensation Disorders (D012678)
..Starting node ..Taste Disorders (D013651)
Child Nodes:
........Ageusia (D000370)
........Dysgeusia (D004408)
........THIOUREA TASTING (OMIM:171200)
Sister Nodes:
..Dizziness (D004244) 1
..Hearing Disorders (D006311) 403
..Olfaction Disorders (D000857) 4
..Posterior column ataxia (C536342)
..Somatosensory Disorders (D020886) 6
..Taste Disorders (D013651) 3
..Vision Disorders (D014786) 84
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10875
Name:	Taste Disorders
Definition:	Conditions characterized by an alteration in gustatory function or perception. Taste disorders are frequently associated with OLFACTION DISORDERS. Additional potential etiologies include METABOLIC DISEASES; DRUG TOXICITY; and taste pathway disorders (e.g., TASTE BUD diseases; FACIAL NERVE DISEASES; GLOSSOPHARYNGEAL NERVE DISEASES; and BRAIN STEM diseases).
Alternative IDs:
ParentIDs:	MESH:D012678
TreeNumbers:	C10.597.751.861 \|C23.888.592.763.861
Synonyms:	Metallic Taste \|Metallic Tastes \|Primary Taste Disorder \|Primary Taste Disorders \|Secondary Taste Disorder \|Secondary Taste Disorders \|Taste Disorder \|Taste Disorder, Anterior Tongue \|Taste Disorder, Posterior Tongue \|Taste Disorder, Primary \|Taste Disorder, Prima
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D013651 MeSH: D013651 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants