Autosome Autosomal recessive cerebellar ataxia type 1 Autosomal dominant cerebellar ataxia Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Autosomal dominant GTP cyclohydrolase I deficiency Autosomal recessive bestrophinopathy Autosomal dominant porencephaly type I Worth syndrome Autosomal recessive axonal neuropathy with neuromyotonia Autosomal recessive multiple epiphyseal dysplasia Autosomal dominant leukodystrophy with autonomic disease Alwadei syndrome Autosomal recessive cerebellar ataxia Autosomal recessive isolated ectopia lenti…

is Prevention of autosomal recessive disorders Autosomal dominant partial epilepsy with auditory features Autosomal dominant multiple pterygium syndrome Woolly hair autosomal recessive Autosomal dominant cerebellar ataxia, deafness, and narcolepsy Craniometaphyseal dysplasia Autosomal recessive spastic ataxia of Charlevoix-Saguenay Cochleosaccular degeneration with progressive cataracts Tetra-amelia syndrome Autosomal dominant nocturnal frontal lobe epilepsy Medullary cystic kidney disease Trisomy Autosomal recessive GTP cyclohydrolase I deficiency Monilethrix Polycystic kidne

y disease 3 (autosomal dominant) CADASIL Bethlem myopathy Microcephaly lymphoedema chorioretinal dysplasia Hypohidrotic ectodermal dysplasia Tyrosine hydroxylase deficiency Robinow syndrome Genealogical DNA test CHAMP1-associated intellectual disability syndrome Nonsyndromic deafness Familial exudative vitreoretinopathy Retinitis pigmentosa Osteopetrosis Autosomal dominant hypophosphatemic rickets Ichthyosis Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome Genetic disorder Dominance (genetics) Polycystic kidney disease Chondrodysplasia punctata Severe congenital neutropen