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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: Substance-Related Disorders (D019966)
..Starting node ..Amphetamine-Related Disorders (D019969)
Child Nodes:
Sister Nodes:
..Alcohol-Related Disorders (D019973) 22
..Amphetamine-Related Disorders (D019969)
..Cocaine-Related Disorders (D019970)
..Drug Overdose (D062787)
..Inhalant Abuse (D058545)
..Marijuana Abuse (D002189)
..Neonatal Abstinence Syndrome (D009357)
..Opioid-Related Disorders (D009293) 2
..Phencyclidine Abuse (D010623)
..Psychoses, Substance-Induced (D011605) 1
..Substance Abuse, Intravenous (D015819)
..Substance Withdrawal Syndrome (D013375) 2
..Tobacco Use Disorder (D014029) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	563
Name:	Amphetamine-Related Disorders
Definition:	Disorders related or resulting from use of amphetamines.
Alternative IDs:
ParentIDs:	MESH:D019966
TreeNumbers:	C25.775.225 \|F03.900.225
Synonyms:	Abuse, Amphetamine \|Addiction, Amphetamine \|Amphetamine Abuse \|Amphetamine Addiction \|Amphetamine Dependence \|Amphetamine Related Disorders \|Dependence, Amphetamine \|Disorder, Amphetamine-Related \|Disorders, Amphetamine-Related
Slim Mappings:	Mental disorder\|Substance-related disorder
Reference:	MedGen: D019969 MeSH: D019969 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants