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Monosomy 9q22.3

MONDO:0019179

Interstitial 9q22.3 microdeletion is associated with a phenotype including macrocephaly, overgrowth and trigonocephaly. Psychomotor delay, hyperactivity and distinctive facial features were also observed. It has been described in two unrelated children.

Also known as: microdeletion 9q22.3

0 clinical trials for this condition and its sub-types, 0 tagged with Monosomy 9q22.3 itself.

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Part of

↑ Partial monosomy of the long arm of chromosome 9 (0)

Including sub-types (0) Tagged with Monosomy 9q22.3 (0)

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