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 Worth syndrome Autosomal dominant porencephaly type I 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 lentis Autosomal domin…

nant partial epilepsy with auditory features Autosomal dominant multiple pterygium syndrome Prevention of autosomal recessive disorders Autosomal dominant cerebellar ataxia, deafness, and narcolepsy Woolly hair autosomal recessive 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 CADASIL Polycystic kidney disease 3 (autosomal dominant) Bethlem myopathy Microcephaly lymphoedema c

horioretinal dysplasia Hypohidrotic ectodermal dysplasia Tyrosine hydroxylase deficiency Robinow syndrome CHAMP1-associated intellectual disability syndrome Familial exudative vitreoretinopathy Genealogical DNA test Nonsyndromic deafness 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 neutropenia Photic sneeze reflex Limb–girdle muscular dystrophy Spastic paraplegia 6 Renal dysplasia-limb defects syndrome Cornea plana 1 Gillespie syndrome