2q32q33 deletion (Q60201)

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Revision as of 07:42, 14 August 2026 by Determinaradmin (talk | contribs) (‎Changed label, description and/or aliases in pt-br, en)
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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ID_2015922071
    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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