general/autosomal-dominant-disorders

3-Methylcrotonyl-CoA carboxylase deficiency (1) Von Willebrand disease (1) Miller–Dieker syndrome (1) Platyspondylic lethal skeletal dysplasia, Torrance type (1) Bethlem myopathy (1) Spondyloepiphyseal dysplasia congenita (1) 3-Methylcrotonyl-CoA carboxylase deficiency (1) Von Hippel–Lindau disease (1) Tricho-rhino-phalangeal syndrome Type 1 (1) Worth syndrome (1) Von Hippel–Lindau disease (1) Weaver syndrome (1) Collagenopathy, types II and XI (1) Von Hippel–Lindau disease (1) Gray platelet syndrome (1) Polydactyly (1) Liddle's syndrome (1) Adermatoglyphia (1) Spinal muscular atrophy with lower extremity predominance 1 (1) Worth syndrome (1) Parastremmatic dwarfism (1) Spinal muscular atrophy with lower extremity predominance 1 (1) MOMO syndrome (1) Albright's hereditary osteodystrophy (1) PAPA syndrome (1) Spinal muscular atrophy with lower extremity predominance 1 (1) Familial atrial fibrillation (1) Singleton Merten syndrome (1) Worth syndrome (1) Buschke–Ollendorff syndrome (1) Vitelliform macular dystrophy (1) Medullary cystic kidney disease (1) Keratolytic winter erythema (1) Hereditary mucoepithelial dysplasia (1) Miller–Dieker syndrome (1) Pelger–Huët anomaly (1) 3-Methylcrotonyl-CoA carboxylase deficiency (1) Von Hippel–Lindau disease (1) Roussy–Lévy syndrome (1) Miller–Dieker syndrome (1) Autosomal dominant cerebellar ataxia (1) Zimmermann–Laband syndrome (1) Spinal muscular atrophy with lower extremity predominance 1 (1) Weaver syndrome (1) Collagenopathy, types II and XI (1) Worth syndrome (1) Miller–Dieker syndrome (1) 3-Methylcrotonyl-CoA carboxylase deficiency (1) Miller–Dieker syndrome (1) Von Hippel–Lindau disease (1)