Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Niemann-Pick disease
ADR ID BADD_A07478
ADR Hierarchy
03      Congenital, familial and genetic disorders
03.08      Metabolic and nutritional disorders congenital
03.08.02      Lysosomal storage disorders
03.08.02.003      Niemann-Pick disease
14      Metabolism and nutrition disorders
14.14      Inborn errors of metabolism
14.14.02      Lysosomal storage disorders
14.14.02.003      Niemann-Pick disease
17      Nervous system disorders
17.16      Demyelinating disorders
17.16.03      Leukodystrophies
17.16.03.001      Niemann-Pick disease
Description A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences. [MeSH]
MedDRA Code 10029403
MeSH ID D009542; D009542; D052536
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Niemann-Pick disease | Sphingomyelin lipidosis | Niemann-Pick Diseases | Niemann Pick Diseases | Niemann-Pick Disease | Niemann Pick Disease
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_D00511Clozapine0.001462%
BADD_D01465Miglustat0.142097%
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