Visual Synonyms
 

Synonyms and Antonyms of genetic disorder

Save this image.
genetic disorder

synonym (synonym of genetic disorder)

hypernym (genetic disorder IS A KIND OF .... relation)

  • a disease or disorder that is inherited genetically (noun.state)
    an impairment of health or a condition of abnormal functioning (noun.state)
     

hyponym (.... IS A KIND OF genetic disorder relation)

  • (noun.state)
    an inherited disease controlled by a single pair of genes (noun.state)
     
  • (noun.state)
    an inherited disease controlled by several genes at once (noun.state)
     
  • (noun.state)
    an inherited skeletal disorder beginning before birth; cartilage is converted to bone resulting in dwarfism (noun.state)
     
  • (noun.state)
    a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and a more.. (noun.state)
     
  • (noun.state)
    any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism (noun.state)
     
  • (noun.state)
    congenital condition in which the colon does not have the normal network of nerves; there is little urge to defecate so the feces accumulate and cause more.. (noun.state)
     
  • (noun.state)
    any of a group of genetic disorders involving a defect in the metabolism of mucopolysaccharides resulting in greater than normal levels of mucopolysac more.. (noun.state)
     
  • (noun.state)
    a genetic disorder characterized by high levels of beta-lipoproteins and cholesterol; can lead to atherosclerosis at an early age (noun.state)
     
  • (noun.state)
    any of several congenital diseases in which the skin is dry and scaly like a fish (noun.state)
     
  • (noun.state)
    an inherited disorder of metabolism in which the urine has a odor characteristic of maple syrup; if untreated it can lead to mental retardation and de more.. (noun.state)
     
  • (noun.state)
    an inherited disease in which abnormal amounts of glycogen accumulate in skeletal muscle; results in weakness and cramping (noun.state)
     
  • (noun.state)
    any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles (noun.state)
     
  • (noun.state)
    congenital condition in which some fingers or toes are missing (noun.state)
     
  • (noun.state)
    congenital condition in which some of the teeth are missing (noun.state)
     
  • (noun.state)
    hereditary disorder in which ossification of the labyrinth of the inner ear causes tinnitus and eventual deafness (noun.state)
     
  • (noun.state)
    a disease caused by a dominant mutant gene on an autosome (noun.state)
     
  • (noun.state)
    a disease caused by the presence of two recessive mutant genes on an autosome (noun.state)
     
  • (noun.state)
    a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow (noun.state)
     
  • (noun.state)
    a congenital progressive disorder of lipid metabolism having an onset at age 5 and characterized by blindness and dementia and early death (noun.state)
     
  • (noun.state)
    a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma (noun.state)
     
  • (noun.state)
    an inherited disorder characterized by an increase in bone density; in severe forms the bone marrow cavity may be obliterated (noun.state)
     
  • (noun.state)
    thickening of the skin (usually unilateral on an extremity) caused by congenital enlargement of lymph vessel and lymph vessel obstruction (noun.state)
     
  • (noun.state)
    a genetic abnormality resulting in short stature (noun.state)
     
  • (noun.state)
    congenital disorder consisting of an inability to digest milk and milk products; absence or deficiency of lactase results in an inability to hydrolyze more.. (noun.state)
     
  • (noun.state)
    a genetic abnormality of metabolism causing abdominal pains and mental confusion (noun.state)
     
  • (noun.state)
    a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain (noun.state)
     
synonym hypernym hyponym congenital disease genetic abnormality genetic defect genetic disease hereditary condition hereditary disease disease monogenic disease monogenic disorder polygenic disease polygenic disorder achondroplasia achondroplasty

Link to this page



Latest Searches

genetic disorder, papaw tree, minute of arc, crimean war, vasoconstrictive, cromorne, minute hand, pin down, yelp, crotalus lepidus, minute book, creep feed, ipidae, cree, tap, minus sign, interpret, styrax japonicum, minuit, eidos,