RS373000965 BMPR1B
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Associated Conditions
Type A2 brachydactyly
Acromesomelic dysplasia 3
Inborn genetic diseases
Pulmonary arterial hypertension
Type A2 brachydactyly
Acromesomelic dysplasia 3
Inborn genetic diseases
Pulmonary arterial hypertension
Other Variants in BMPR1B