Fryns syndrome (Q94176): Difference between revisions
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Revision as of 09:18, 16 August 2026
Fryns syndrome is a multiple congenital anomaly syndrome characterised by diaphragmatic hernia, unusual facies, and distal limb hypoplasia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1327847749 |
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| English | Fryns syndrome |
Fryns syndrome is a multiple congenital anomaly syndrome characterised by diaphragmatic hernia, unusual facies, and distal limb hypoplasia. |
Statements
CID11:ID_1327847749
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