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6p22 microdeletion syndrome

MONDO:0016655

6p22 microdeletion syndrome is a newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations.

Also known as: Del(6)(p22), monosomy 6p22

0 clinical trials for this condition and its sub-types, 0 tagged with 6p22 microdeletion syndrome itself.

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Part of

↑ Partial deletion of the short arm of chromosome 6 (0)

Including sub-types (0) Tagged with 6p22 microdeletion syndrome (0)

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