Autosomal dominant disorder - Sanjay Manohar's Medical Browser
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
Type item name:
Sanjay Manohar
2006