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BRWD3 - bromodomain and WD repeat domain containing 3
Diseases list
- Disease-causing germline mutation(s) in Non-specific syndromic intellectual disability
ORPHA:528084 
- Disease-causing germline mutation(s) (loss of function) in NON RARE IN EUROPE: FG syndrome phenotypic spectrum
ORPHA:323
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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