14q11.2 deletion (Q104790): Difference between revisions
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Revision as of 10:39, 17 August 2026
14q11.2 microdeletion syndrome is a chromosomal anomaly syndrome characterised by developmental delay, hypotonia and facial dysmorphism (widely-spaced eyes, short nose with flat nasal bridge, long philtrum, prominent Cupid's bow, full lower lip and auricular anomalies).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1854856553 |
||
| English | 14q11.2 deletion |
14q11.2 microdeletion syndrome is a chromosomal anomaly syndrome characterised by developmental delay, hypotonia and facial dysmorphism (widely-spaced eyes, short nose with flat nasal bridge, long philtrum, prominent Cupid's bow, full lower lip and auricular anomalies). |
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CID11:ID_1854856553
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dki-india-ID_1854856553
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