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Dias-Logan syndrome
rareAny BAFopathy in which the cause of the disease is a mutation in the BCL11A gene.
- Identifiers
- MONDO:0014914 OMIM:617101Orphanet:619233
- Causal genes
- BCL11A
- Part of
- BAFopathySyndromic disease
- Also known as
- BCL11A-related BAFopathy · BCL11A-related intellectual developmental disorder with persistence of fetal hemoglobin · BCL11A-related intellectual developmental disorder with persistence of foetal haemoglobin · Dias-Logan syndrome; DILOS · DILOS
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