Fryns syndrome (Q94176)
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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 |
||
| 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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dki-india-ID_1327847749
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Concluído
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15 August 2026
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