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Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities

MONDO:0060763

Any BAFopathy in which the cause of the disease is a mutation in the BCL11B gene.

Also known as: BCL11B-related disorder, BCL11B-related BAFopathy, intellectual developmental disorder with dysmorphic facies, speech delay, and t-cell abnormalities, IDDSFTA, INTELLECTUAL developmental disorder with speech delay, DYSMORPHIC facies, and T-cell abnormalities

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities itself.

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↑ Autosomal dominant syndromic intellectual disability (15) ↑ BAFopathy (0)

Including sub-types (0) Tagged with Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities (0)

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