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Up to: Hereditary disease

BAFopathy

Disorder caused by mutations in the various subunits composing the BAF complex.

0 trials tagged with this condition →

  • ACTL6A-related BAFopathy 0 trials
  • Baraitser-Winter syndrome 1 0 trials
  • Coffin-Siris syndrome 1 0 trials
  • Coffin-Siris syndrome 5 0 trials
  • Coffin-Siris syndrome 6 0 trials
  • Coffin-Siris syndrome 8 0 trials
  • Dias-Logan syndrome 0 trials
  • PBRM1-related BAFopathy 0 trials
  • SMARCC1-associated developmental dysgenesis syndrome 0 trials
  • Intellectual developmental disorder with severe speech and ambulation defects 0 trials
  • Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities 0 trials
  • Intellectual disability, autosomal dominant 14 0 trials
  • Intellectual disability, autosomal dominant 15 0 trials
  • Intellectual disability, autosomal dominant 16 0 trials
  • Intellectual disability-sparse hair-brachydactyly syndrome 0 trials

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