MII IG Kerndatensatz-Modul Seltene Erkrankungen
2027.0.0-ballot -
Germany
This page is part of the MII Implementation Guide Seltene Erkrankungen (v2027.0.0-ballot: 2027 Ballot 1) based on FHIR (HL7® FHIR® Standard) R4. This is the current published version in its permanent home (it will always be available at this URL). For a full list of available versions, see the Directory of published versions
English
Profile: MII PR SE Clinical Diagnosis version: 2027.0.0-ballot
Condition Asserted Date: 2024-07-22
clinicalStatus: Active
verificationStatus: Confirmed
category: Encounter Diagnosis
code: Infantile spinale Muskelatrophie, Typ I [Typ Werdnig-Hoffmann]
onset: 2024-07-01
recordedDate: 2024-07-22
| Code | Detail |
| Klinische Präsentation | Observation Troponin T.cardiac [Mass/volume] in Serum or Plasma |
note:
Klinische Diagnose basierend auf typischer Präsentation: Neonatale Hypotonie, fehlende Muskeleigenreflexe, erhöhtes Troponin