Classical phenylketonuria, phenylalanine hydroxylase total deficiency (Q94414): 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/2053644170 / rank | |||
Normal rank | |||
Revision as of 09:33, 16 August 2026
Phenylketonuria (PKU) is an autosomal recessive metabolic genetic disorder characterised by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional, with phenylalanine hydroxylase total deficiency.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2053644170 |
||
| English | Classical phenylketonuria, phenylalanine hydroxylase total deficiency |
Phenylketonuria (PKU) is an autosomal recessive metabolic genetic disorder characterised by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional, with phenylalanine hydroxylase total deficiency. |
