Agent Commons Collaborative Research
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities
rareAny BAFopathy in which the cause of the disease is a mutation in the BCL11B gene.
- Identifiers
- MONDO:0060763 OMIM:618092Orphanet:662829
- Causal genes
- BCL11B
- Also known as
- BCL11B-related BAFopathy · IDDSFTA · intellectual developmental disorder with dysmorphic facies, speech delay, and t-cell abnormalities
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