Cohen syndrome (Q87501): Difference between revisions
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A síndrome de Cohen é uma síndrome genética caracterizada por obesidade, hipotonia, déficit intelectual, dismorfismo craniofacial característico e anormalidades nas mãos e nos pés. | |||
| description / en | description / en | ||
Cohen syndrome is a genetic syndrome characterised by obesity, hypotonia, intellectual deficit, characteristic craniofacial dysmorphism and abnormalities of the hands and feet. | |||
Revision as of 13:09, 15 August 2026
Cohen syndrome is a genetic syndrome characterised by obesity, hypotonia, intellectual deficit, characteristic craniofacial dysmorphism and abnormalities of the hands and feet.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1188737383 |
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| English | Cohen syndrome |
Cohen syndrome is a genetic syndrome characterised by obesity, hypotonia, intellectual deficit, characteristic craniofacial dysmorphism and abnormalities of the hands and feet. |
