Malignant hyperphenylalaninaemia due to tetrahydrobiopterin deficiency (Q93272): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 08:22, 16 August 2026
This condition is characterised by mildly or strongly elevated levels of the amino acid phenylalanine in the blood. This diagnosis is due to a rare metabolic disorder that increases the blood levels of phenylalanine.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1659163210 |
||
| English | Malignant hyperphenylalaninaemia due to tetrahydrobiopterin deficiency |
This condition is characterised by mildly or strongly elevated levels of the amino acid phenylalanine in the blood. This diagnosis is due to a rare metabolic disorder that increases the blood levels of phenylalanine. |
Statements
CID11:ID_1659163210
0 references
dki-india-ID_1659163210
0 references
Concluído
0 references
15 August 2026
0 references
