Autosomal dominant disorder

external

• Parents

  • Genetic disease

• Children

  • Achondroplasia
  • Huntington disease
  • Adult polycystic kidney disease
  • Von Hippel-Lindau disease
  • Marfan syndrome
  • Retinoblastoma
  • Charcot-Marie-Tooth syndrome
  • Myotonic dystrophy
  • Hypertrophic cardiomyopathy
  • Hereditary haemorrhagic telangiectasia
  • Hereditary spherocytosis
  • Von Willebrand disease
  • Peutz-Jegher syndrome
  • Familial adenomatous polyposis coli
  • Gardener's syndrome
  • Multiple endocrine neoplasia syndrome
  • Type II polyglandular syndrome
  • Type III polyglandular syndrome
  • Neurofibromatosis
  • Medullary thyroid cancer
  • Retinitis pigmentosa
  • Osteogenesis imperfecta
  • Osteopetrosis
  • Cranio-cleido dysostosis
  • Phakomatosis
  • Hereditary angioedema
  • Malignant hyperpyrexia
  • Autosomal dominant congenital metabolic disease
  • Alagille syndrome
  • Alport syndrome
  • Apert syndrome
  • Beckwith-Wiedemann syndrome
  • Birt-Hogg-Dube Syndrome
  • Ehlers-Danlos syndrome
  • Erb's muscular dystrophy
  • Holt-Oram syndrome
  • Howel-Evans syndrome
  • Li-Fraumeni syndrome
  • Job syndrome
  • Rubinstein-Taybi syndrome
  • Sturge-Weber syndrome
  • Treacher Collins syndrome
  • Ward-Romano syndrome
  • Williams syndrome
  • Wolff-Parkinson-White syndrome
  • Spinocerebellar ataxia
  • Olivopontocerebellar degeneration
  • Myotonia congenita
  • Torsion dystonia
  • Central core myopathy
  • Centronuclear myopathy
  • Tau protein mutation
  • Facioscapulohumeral dystrophy
  • Hereditary motor and sensory neuropathy type I
  • Familial amyloidotic polyneuropathy
  • Benign essential tremor
  • Tuberous sclerosis
  • Pseudoxanthoma elasticum
  • Doyne honeycomb retinal dystrophy
  • Fuch's dystrophy
  • Acanthosis nigricans
  • Cutis laxa
  • Dysplastic Naevus
  • Darier disease
  • Ichthyosis vulgaris
  • Tylosis
  • Cerebral autosomal dominant angiopathy with subcortical infarcts and leucoencephalopathy
  • Schnyder corneal dystrophy