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2q31.1 microdeletion syndrome

MONDO:0016652

2q31.1 microdeletion syndrome is a well-defined and clinically recognizable syndrome characterized by moderate to severe developmental delay, short stature, facial dysmorphism and variable limb defects.

Also known as: Del(2)(q31.1), monosomy 2q31.1

0 clinical trials for this condition and its sub-types, 0 tagged with 2q31.1 microdeletion syndrome itself.

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Part of

↑ Partial deletion of the long arm of chromosome 2 (2)

Including sub-types (0) Tagged with 2q31.1 microdeletion syndrome (0)

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