16p13.11 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, epilepsy, short stature, facial dysmorphism and behavioral problems.
Comprehensive, easy-to-understand information about this condition
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chromosome 16p12.1 deletion syndrome, 520kb
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alpha thalassemia-intellectual disability syndrome type 1
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autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
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proximal 16p11.2 microdeletion syndrome
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distal 16p11.2 microdeletion syndrome
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chromosome 16p12.2-p11.2 deletion syndrome
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