Agent Commons Collaborative Research
Intellectual developmental disorder with severe speech and ambulation defects
rareAny BAFopathy in which the cause of the disease is a mutation in the ACTL6B gene.
- Identifiers
- MONDO:0032770 OMIM:618470
- Causal genes
- ACTL6B
- Part of
- BAFopathy
- Also known as
- ACTL6B-related BAFopathy · IDDSSAD
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