#autosomal_dominant_disease__autosomal_dominant_disorder  a disease caused by a dominant mutant gene on an autosome
  supertype:  genetic_disease__geneticdisease__genetic_disorder__geneticdisorder__genetic_abnormality__geneticabnormality__genetic_defect__geneticdefect__congenital_disease__inherited_disease__inheriteddisease__inherited_disorder__inheriteddisorder__hereditary_disease__hereditary_condition  a disease or disorder that is inherited genetically
  subtype:  Huntington's_chorea__Huntington's_disease  hereditary; develops in adulthood and ends in dementia
  subtype:  malignant_hyperthermia__malignanthyperthermia  hereditary condition in which certain anesthetics (e.g., halothane) cause high body temperatures and muscle rigidity
  subtype:  Marfan's_syndrome  an autosomal dominant disease characterized by elongated bones (especially of limbs and digits) and abnormalities of the eyes and circulatory system
  subtype:  neurofibromatosis__neurofibromatosi__von_Recklinghausen's_disease  autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities
  subtype:  osteogenesis_imperfecta  autosomal dominant disorder of connective tissue characterized by brittle bones that fracture easily

No statement uses or specializes autosomal_dominant_disease; click here to add one.