19p13.12 microdeletion syndrome

MONDO:0016765

19p13.12 microdeletion syndrome is a newly described syndrome characterized by moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism.

Also known as: Del(19)(p13.12), monosomy 19p13.12, Chromosome19p13.12 microdeletion

0 clinical trials for this condition and its sub-types, 0 tagged with 19p13.12 microdeletion syndrome itself.

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Part of

↑ Partial deletion of the short arm of chromosome 19 (0)

Including sub-types (0) Tagged with 19p13.12 microdeletion syndrome (0)

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