Disease

chromosome 16q22 deletion syndrome

Definition
A chromosomal deletion syndrome that has_material_basis_in an interstitial 16q22 deletion that is characterized by a failure to thrive in infancy, poor growth, delayed psychomotor development, hypotonia, and dysmorphic features, including large anterior fontanel, high forehead, diastasis of the cranial sutures, broad nasal bridge, hypertelorism, low-set abnormal ears, and short neck.
Synonyms
None
Cross References
Parent Terms
Child Terms
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Sources of Associations

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      Associated Models

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