Overview
NOCARH syndrome is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Autosomal dominant hereditary disorder(parent)
Type I interferonopathy(parent)
Neonatal anemia(parent)
Haemophagocytic lymphohistiocytosis(parent)
Inherited platelet disorder(parent)
Disorder of hematopoietic system in newborn(parent)
Hereditary white blood cell disorder(parent)
Acquired pancytopenia(parent)
Neonatal thrombocytopenia(parent)
Quick Facts
- SNOMED CT
- 1360083000
- UMLS CUI
- C5925147
- Fully Specified Name
- Neonatal onset cytopenia, autoinflammation, rash, episodes of hemophagocytic lymphohistiocytosis syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.