Peroxisomal D-bifunctional enzyme deficiency (Q88702): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/996981847 / rank
 
Normal rank

Revision as of 15:05, 15 August 2026

This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes.
Language Label Description Also known as
default for all languages
ID_996981847
    English
    Peroxisomal D-bifunctional enzyme deficiency
    This refers to the autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific peroxisomal enzymes.

      Statements