| / English Dictionary |
INHERITED DISORDER
| Pronunciation (US): |  | (GB): | |
I. (noun)
Sense 1
Meaning:
A disease or disorder that is inherited genetically
Synonyms:
congenital disease; genetic abnormality; genetic defect; genetic disease; genetic disorder; hereditary condition; hereditary disease; inherited disease; inherited disorder
Classified under:
Nouns denoting stable states of affairs
Hypernyms ("inherited disorder" is a kind of...):
disease (an impairment of health or a condition of abnormal functioning)
Hyponyms (each of the following is a kind of "inherited disorder"):
hepatolenticular degeneration; Wilson's disease (a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain)
porphyria (a genetic abnormality of metabolism causing abdominal pains and mental confusion)
lactase deficiency; lactose intolerance; milk intolerance (congenital disorder consisting of an inability to digest milk and milk products; absence or deficiency of lactase results in an inability to hydrolyze lactose)
dwarfism; nanism (a genetic abnormality resulting in short stature)
nevoid elephantiasis; pachyderma (thickening of the skin (usually unilateral on an extremity) caused by congenital enlargement of lymph vessel and lymph vessel obstruction)
Albers-Schonberg disease; marble bones disease; osteopetrosis (an inherited disorder characterized by an increase in bone density; in severe forms the bone marrow cavity may be obliterated)
congenital afibrinogenemia (a rare congenital disorder of blood coagulation in which no fibrinogen is found in the blood plasma)
juvenile amaurotic idiocy; Spielmeyer-Vogt disease (a congenital progressive disorder of lipid metabolism having an onset at age 5 and characterized by blindness and dementia and early death)
congenital pancytopenia; Fanconi's anaemia; Fanconi's anemia (a rare congenital anemia characterized by pancytopenia and hypoplasia of the bone marrow)
autosomal recessive defect; autosomal recessive disease (a disease caused by the presence of two recessive mutant genes on an autosome)
autosomal dominant disease; autosomal dominant disorder (a disease caused by a dominant mutant gene on an autosome)
otosclerosis (hereditary disorder in which ossification of the labyrinth of the inner ear causes tinnitus and eventual deafness)
oligodontia (congenital condition in which some of the teeth are missing)
oligodactyly (congenital condition in which some fingers or toes are missing)
dystrophy; muscular dystrophy (any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles)
McArdle's disease (an inherited disease in which abnormal amounts of glycogen accumulate in skeletal muscle; results in weakness and cramping)
branched chain ketoaciduria; maple syrup urine disease (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 death in early childhood)
ichthyosis (any of several congenital diseases in which the skin is dry and scaly like a fish)
hyperbetalipoproteinemia (a genetic disorder characterized by high levels of beta-lipoproteins and cholesterol; can lead to atherosclerosis at an early age)
mucopolysaccharidosis (any of a group of genetic disorders involving a defect in the metabolism of mucopolysaccharides resulting in greater than normal levels of mucopolysaccharides in tissues)
congenital megacolon; Hirschsprung's disease (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 megacolon)
inborn error of metabolism (any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism)
abetalipoproteinemia (a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels)
achondroplasia; achondroplasty; chondrodystrophy; osteosclerosis congenita (an inherited skeletal disorder beginning before birth; cartilage is converted to bone resulting in dwarfism)
polygenic disease; polygenic disorder (an inherited disease controlled by several genes at once)
monogenic disease; monogenic disorder (an inherited disease controlled by a single pair of genes)
Context examples:
A rare, inherited disorder marked by a buildup in the liver of bile (fluid that helps digest fat).
(PFIC, NCI Dictionary)
An inherited disorder that causes a build-up of phenylalanine (an amino acid) in the blood.
(Phenylketonuria, NCI Dictionary)
A very rare, autosomal recessive inherited disorder caused by deficiency of the enzyme phosphoenolpyruvate carboxykinase, which is involved in gluconeogenesis.
(Phosphoenolpyruvate Carboxykinase Deficiency, NCI Thesaurus)
A rare autosomal recessive inherited disorder caused by mutations in the cathepsin C gene.
(Papillon-Lefevre Syndrome, NCI Thesaurus)
A rare autosomal recessive inherited disorder caused by mutations in the PANK2 gene.
(Pantothenate Kinase-Associated Neurodegeneration, NCI Thesaurus)
An autosomal dominant inherited disorder caused by mutations in the PABPN1 gene.
(Oculopharyngeal Muscular Dystrophy, NCI Thesaurus)
A rare autosomal dominant inherited disorder characterized by the presence of small areas of increased density throughout the bones.
(Osteopoikilosis, NCI Thesaurus)
A very rare autosomal dominant inherited disorder caused by mutations in the GLI3 gene.
(Pallister-Hall Syndrome, NCI Thesaurus)
An inherited disorder characterized by the development of keratotic lesions on the palms and soles.
(Diffuse Palmoplantar Keratoderma, NCI Thesaurus)
An inherited disorder in which a person doesn’t have enough of an enzyme called G6PD that helps red blood cells work the way they should.
(G6PD Deficiency, NCI Dictionary)
YOU MAY ALSO LIKE
