MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot -
Germany
MII IG Kerndatensatz-Modul Seltene Erkrankungen - Downloaded Version 2027.0.0-ballot See the Directory of published versions
English
Profile: MII PR SE Genetic Diagnosis version: 2027.0.0-ballot
clinicalStatus: Active
verificationStatus: Confirmed
category: Genetic disease
code: Phenylketonurie
recordedDate: 2024-01-01
| Code | Detail |
| PAH-Gen Mutation c.1222C>T (p.R408W) | Observation Genetic variant assessment |
note:
Klassische PKU mit PAH-Gen Mutation c.1222C>T, erfordert lebenslange phenylalaninarme Diät