Diseases by Functional categories

DISEASE	FUNCTIONAL CATEGORY
Acatalasemia	Antioxidant Catalase
Acyl-CoA oxidase deficiency (Pseudoneonatal adrenoleukodystrophy)	Branched chain fatty acid beta-oxidation Branched chain fatty acid oxidation Di- trihydroxycholestanoic acid beta-oxidation Di- trihydroxycholestanoic acid oxidation/Bile acid synthesis Fatty acid oxidation Fatty acid synthesis/PUFAS synthesis Long-chain dicarboxylic acids oxidation Straight chain fatty acids beta-oxidation Straight chain fatty acids oxidation Unsaturated fatty acid beta-oxidation
Adult-onset sensory motor neuropathy	Branched chain fatty acid oxidation Di- trihydroxycholestanoic acid oxidation/Bile acid synthesis Fatty acid oxidation
Amyotrophic lateral sclerosis, ALS1	Antioxidant Superoxide dismutase
Bifunctional protein deficiency	Branched chain fatty acid beta-oxidation Branched chain fatty acid oxidation Di- trihydroxycholestanoic acid beta-oxidation Di- trihydroxycholestanoic acid oxidation/Bile acid synthesis Fatty acid oxidation Fatty acid synthesis/PUFAS synthesis Long-chain dicarboxylic acids oxidation Straight chain fatty acids beta-oxidation Straight chain fatty acids oxidation Unsaturated fatty acid beta-oxidation
Contiguous ABCD1/DXS1375E deletion syndrome	ABC transporters Di- trihydroxycholestanoic acid oxidation/Bile acid synthesis Fatty acid oxidation Fatty acid synthesis/PUFAS synthesis Lipid metabolism Peroxisomal membrane proteins (PMP) Straight chain fatty acids oxidation
Glomerulosclerosis	Peroxisomal membrane proteins (PMP) PXMP 2/4 family proteins
Glutaric aciduria type III	No role found
Hyperoxaluria type I	Carbohydrate Metabolism Metabolism Protein/amino acid metabolism Transaminases
Infantile Refsum disease	Peroxisomal AAA-ATPases Peroxisome biogenesis (peroxins) Peroxisome matrix protein import Peroxisome targeting sequence binding ZN RING proteins
Malonic aciduria	Fatty acid oxidation Lipid metabolism
Mental retardation X-linked 63, MRX63	Lipid metabolism Long/very long fatty acids activation
Mulibrey nanism	Classification Unknown
Neonatal adrenoleukodystrophy	Peroxisomal AAA-ATPases Peroxisome biogenesis (peroxins) Peroxisome docking Peroxisome matrix protein import Peroxisome membrane assembly Peroxisome targeting sequence binding ZN RING proteins
Refsum disease	Alpha-oxidation Branched chain fatty acid oxidation Peroxisome biogenesis (peroxins) Peroxisome targeting sequence binding
Rhizomelic chondrodysplasia punctata type 1 (RCDP1 )	Peroxisome biogenesis (peroxins) Peroxisome targeting sequence binding
Rhizomelic chondrodysplasia punctata type 2 (RCDP2)	Etherlipid and plasmalogens synthesis Lipid metabolism
Rhizomelic chondrodysplasia punctata type 3 (RCDP3)	Etherlipid and plasmalogens synthesis Lipid metabolism
Sjogren-Larsson syndrome	No role found
X-linked adrenoleukodystrophy	ABC transporters Di- trihydroxycholestanoic acid oxidation/Bile acid synthesis Fatty acid oxidation Fatty acid synthesis/PUFAS synthesis Lipid metabolism Peroxisomal membrane proteins (PMP) Straight chain fatty acids oxidation
Xanthinuria	Metabolism Purines and pyrimidines
Zellweger syndrome	Peroxisomal AAA-ATPases Peroxisome biogenesis (peroxins) Peroxisome docking Peroxisome matrix protein import Peroxisome membrane assembly Peroxisome targeting sequence binding ZN RING proteins