FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term peroxisomal disease ID (Ontology) DOID:906 (Human Disease)
Definition An inherited metabolic disorder that involves peroxisome malfunction.
Also Known As "peroxisomal disorder"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       4
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 peroxisomal disease       4      3
 model of | peroxisomal disease       4       --
Spanning Tree (Parents/Children)
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disease of metabolism__
genetic disease________|
                       inherited metabolic disorder
                        |__peroxisomal disease  79 rec.
                            |__acatalasia 2 rec.
                            |__alpha-methylacyl-CoA racemase deficiency 1 rec.
                            |__D-bifunctional protein deficiency 1 rec.
                            |__glutaric acidemia type 3 1 rec.
                            |__infantile Refsum disease
                            |__mevalonic aciduria 1 rec.
                            |__Mitchell syndrome 12 rec.
                            |__peroxisomal acyl-CoA oxidase deficiency 5 rec.
                            |__peroxisomal biogenesis disorder 56 rec.
                            |   |__Heimler syndrome 1 1 rec.
                            |   |__Heimler syndrome 2 1 rec.
                            |   |__peroxisome biogenesis disorder 1B 3 rec.
                            |   |__peroxisome biogenesis disorder 2B 1 rec.
                            |   |__peroxisome biogenesis disorder 3B 1 rec.
                            |   |__Peroxisome biogenesis disorder 4B 1 rec.
                            |   |__Peroxisome biogenesis disorder 5B 1 rec.
                            |   |__Peroxisome biogenesis disorder 6B 1 rec.
                            |   |__Peroxisome biogenesis disorder 7B
                            |   |__Peroxisome biogenesis disorder 8B 1 rec.
                            |   |__Peroxisome biogenesis disorder 9B 3 rec.
                            |   |__Peroxisome biogenesis disorder 10B 1 rec.
                            |   |__Peroxisome biogenesis disorder 11B 1 rec.
                            |   |__peroxisome biogenesis disorder 14B 2 rec.
                            |   |__Zellweger syndrome(+) 47 rec.
                            |__retinal dystrophy with leukodystrophy 1 rec.
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Is a inherited metabolic disorder
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Synonyms
  • "peroxisomal disorder" EXACT
Secondary IDs
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ICD10CM:E71.5
ICD9CM:277.86
MESH:D018901
NCI:C85005
SNOMEDCT_US_2023_03_01:238059005
UMLS_CUI:C0282528