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ROR2 - receptor tyrosine kinase like orphan receptor 2
Diseases list
- Disease-causing germline mutation(s) (loss of function) in Autosomal recessive Robinow syndrome
ORPHA:1507 - Disease-causing germline mutation(s) (gain of function) in Brachydactyly type B
ORPHA:93383

Additional information
Health care resources for this gene
Research activities on this gene
Specialised Social Services
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