Fryns syndrome

Preferred Label : Fryns syndrome;

ICD-11 definition : Fryns syndrome is a multiple congenital anomaly syndrome characterized by diaphragmatic hernia, unusual facies, and distal limb hypoplasia.;

Details

Origin ID

1327847749;

Automatic exact mappings (from CISMeF team)
- Diaphragmatic hernia, abnormal face and distal limb anomalies (disorder) [SNOMED CT concept]
- Fryns Syndrome [NCIt concept]
- Fryns syndrome [OMIM Phenotype]
- Fryns syndrome [PASCAL descriptor]
- Fryns syndrome [MedDRA Preferred Term]
- Fryns syndrome [MeSH concept]
- Fryns syndrome [ORDO Disease]
- fryns syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients