Fryns syndrome (Q94176): Difference between revisions
From determinar.ia.br - Determine suas informações
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Síndrome de Fryns é uma síndrome de anomalia congênita múltipla caracterizada por hérnia diafragmática, fácies incomum e hipoplasia distal de membro. | |||
| description / en | description / en | ||
Fryns syndrome is a multiple congenital anomaly syndrome characterised by diaphragmatic hernia, unusual facies, and distal limb hypoplasia. | |||
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. |
