19p13.12 deletion (Q65356)
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19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1258292853 |
||
| English | 19p13.12 deletion |
19p13.12 microdeletion syndrome is a chromosomal anomaly associated with moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism. |
Statements
CID11:ID_1258292853
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dki-india-ID_1258292853
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Concluído
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13 August 2026
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