SYNGAP1 syndrome (Q101738)
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A neurodevelopmental encephalopathy notable for intellectual deficit with clear aetiology from a pathogenic variant of SYNGAP1.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1830660574 |
||
| English | SYNGAP1 syndrome |
A neurodevelopmental encephalopathy notable for intellectual deficit with clear aetiology from a pathogenic variant of SYNGAP1. |
Statements
CID11:ID_1830660574
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dki-india-ID_1830660574
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Concluído
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15 August 2026
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