Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Huntington's disease
ADR ID BADD_A09078
ADR Hierarchy
03      Congenital, familial and genetic disorders
03.10      Neurological disorders congenital
03.10.01      Neurological disorders congenital NEC
03.10.01.009      Huntington's disease
17      Nervous system disorders
17.01      Movement disorders (incl parkinsonism)
17.01.01      Choreiform movements
17.01.01.005      Huntington's disease
Description A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) [MeSH]
MedDRA Code 10070668
MeSH ID D006816; D006816; D006816
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Huntington's chorea | Huntington's chorea aggravated | Huntington's disease | Huntington Disease | Huntington Chorea | Chorea, Huntington | Huntington's Disease | Chronic Progressive Hereditary Chorea (Huntington) | Huntington Chronic Progressive Hereditary Chorea | Progressive Chorea, Chronic Hereditary (Huntington) | Progressive Chorea, Hereditary, Chronic (Huntington) | Huntington's Chorea | Chorea, Huntington's | Chorea, Chronic Progressive Hereditary (Huntington) | Huntington Disease, Late Onset | Late-Onset Huntington Disease | Huntington Disease, Late-Onset | Late Onset Huntington Disease | Juvenile Huntington Disease | Juvenile-Onset Huntington Disease | Juvenile Onset Huntington Disease | Huntington Disease, Juvenile-Onset | Huntington Disease, Juvenile Onset | Huntington Disease, Juvenile | Akinetic-Rigid Variant of Huntington Disease | Akinetic Rigid Variant of Huntington Disease | Huntington Disease, Akinetic-Rigid Variant | Huntington Disease, Akinetic Rigid Variant
ADR Related Proteins
Protein Name UniProt AC TTD Target ID
Not AvailableNot AvailableNot Available
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00165Aripiprazole0.000100%
BADD_D00511Clozapine0.010966%
BADD_D01951Risperidone0.000140%
BADD_D02010Sertraline0.000091%
BADD_D02175Tetrabenazine0.007502%
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