2q31.1 deletion (Q95871): Difference between revisions
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15 August 2026
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Latest revision as of 11:42, 16 August 2026
2q31.1 microdeletion syndrome is a well-defined and clinically recognisable syndrome characterised by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects ranging from monodactylous ectrodactyly, brachydactyly and syndactyly to camptodactyly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_491362822 |
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| English | 2q31.1 deletion |
2q31.1 microdeletion syndrome is a well-defined and clinically recognisable syndrome characterised by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects ranging from monodactylous ectrodactyly, brachydactyly and syndactyly to camptodactyly. |
Statements
CID11:ID_491362822
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dki-india-ID_491362822
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Concluído
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15 August 2026
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