8p11.2 deletion syndrome

MONDO:0016657

8p11.2 deletion syndrome is a contiguous gene syndrome characterized by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.

Also known as: Del(8)(p11.2), monosomy 8p11.2

0 clinical trials for this condition and its sub-types, 0 tagged with 8p11.2 deletion syndrome itself.

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Part of

↑ Partial deletion of the short arm of chromosome 8 (0)

Including sub-types (0) Tagged with 8p11.2 deletion syndrome (0)

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