amino acid metabolic disorder
MeSH: D000592ORPHA: 79062
Overview
inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
D000592Orphanet Code
ORPHA:79062amino acid metabolic disorder
| MeSH | D000592 |
| Orphanet | ORPHA:79062 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO