RS147952898 PDGFRB
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Associated Conditions
Inborn genetic diseases
Infantile myofibromatosis
Acroosteolysis-keloid-like lesions-premature aging syndrome
Basal ganglia calcification
idiopathic
4
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome
Inborn genetic diseases
Infantile myofibromatosis
Acroosteolysis-keloid-like lesions-premature aging syndrome
Basal ganglia calcification
idiopathic
4
Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome
Other Variants in PDGFRB