SATB2 associated disorder

MONDO:0100147

A syndromic intellectual disability disorder that is characterized by significant neurodevelopmental disabilities with limited to absent speech, behavioral issues, and craniofacial anomalies. Most distinctive features are neurodevelopmental with invariably severely limited speech, cleft or high arched palate, dental anomalies (crowding, macrodontia, abnormal shape), and behavioral issues with or without bone or brain anomalies.

Also known as: SAS, SATB2 associated disorder, SATB2-associated syndrome

1 clinical trial for this condition and its sub-types, 0 tagged with SATB2 associated disorder itself.

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Part of

↑ Autosomal dominant syndromic intellectual disability (15)

Sub-types of SATB2 associated disorder

Chromosome 2q32-q33 deletion syndrome 1 trial

Including sub-types (1) Tagged with SATB2 associated disorder (0)

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