2q32q33 deletion (Q60201): Difference between revisions
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Revision as of 07:42, 14 August 2026
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.
| Language | Label | Description | Also known as |
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| default for all languages | ID_2015922071 |
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| English | 2q32q33 deletion |
2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features. |
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CID11:ID_2015922071
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dki-india-ID_2015922071
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