#autosomal_recessive_disease__autosomalrecessivedisease__autosomal_recessive_defect__autosomalrecessivedefect  a disease caused by the presence of two recessive mutant genes 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:  limb-girdle_muscular_dystrophy  an autosomal recessive form of muscular dystrophy characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle
  subtype:  Niemann-Pick_disease  a disorder of lipid metabolism that is inherited as an autosomal recessive trait
  subtype:  Tay-Sachs_disease__Tay-Sachs__Sachs_disease__infantile_amaurotic_idiocy__infantileamauroticidiocy  a hereditary disorder of lipid metabolism occuring most frequently in individuals of E European Jewish descent; accumulation of lipids in nervous tissue results in death in early childhood
  subtype:  thrombasthenia  a rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results
  subtype:  tyrosinemia  autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation
  subtype:  Werdnig-Hoffman_disease  autosomal recessive disease in which the degeneration of spinal nerve cells and brain nerve cells leads to atrophy of skeletal muscles and flaccid paralysis; death usually occurs in early childhood

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