tyrosinemia type II
ICD-10: E70.2ORPHA: 69723
Overview
tyrosinemia that has material basis in deficiency of hepatic tyrosine aminotransferase located in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
ICD-10 Code
E70.2Orphanet Code
ORPHA:69723tyrosinemia type II
| ICD-10 | E70.2 |
| Orphanet | ORPHA:69723 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO