Loss of single peroxisomal function

Loss of single peroxisomal function (disorder)

active

Code	`238066006`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20020131

Parents (1)

238059005Disorder of peroxisomal function disorder

Children (13)

267454002Acatalasaemia disorder
238069004Acyl-CoA oxidase deficiency disorder
65389002Adrenoleucodystrophy disorder
238068007Bifunctional peroxisomal enzyme deficiency disorder
773415005Contiguous ABCD1 DXS1357E deletion syndrome disorder
238071004Dihydroxycholestanoic acidaemia and trihydroxycholestanoic acidaemia disorder
1237619001Fatty acyl-CoA reductase 1 deficiency disorder
238070003Glutaryl-CoA oxidase deficiency disorder
238073001Isolated alkyldihydroxyacetone phosphate synthase deficiency disorder
238072006Isolated dihydroxyacetone phosphate acyltransferase deficiency disorder
733452000Leucoencephalopathy, dystonia, motor neuropathy syndrome disorder
238067002Peroxisomal thiolase deficiency disorder
65520001Primary hyperoxaluria, type I disorder