19p13.12 deletion (Q65356): Difference between revisions
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Revision as of 13:04, 14 August 2026
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 |
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| default for all languages | ID_1258292853 |
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| 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. |
