Hyperonyms
(has_hyperonym)
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14151139-n:
a disease or disorder that is inherited genetically
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Hyponyms
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14128812-n:
a congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of life
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Hyponyms
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14155506-n:
the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; no cure is known
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Hyponyms
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14156345-n:
a rare chronic disorder of lipid metabolism of genetic origin
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Hyponyms
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14156976-n:
hereditary disease; develops in adulthood and ends in dementia
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Hyponyms
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14157163-n:
hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation
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Hyponyms
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14158179-n:
autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities
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Hyponyms
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14168792-n:
a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
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Hyponyms
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14169364-n:
a hereditary disorder of lipid metabolism occurring most frequently in individuals of Jewish descent in eastern Europe; accumulation of lipids in nervous tissue results in death in early childhood
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Hyponyms
(has_hyponym)
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14195715-n:
an inherited form of anemia caused by faulty synthesis of hemoglobin
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Hyponyms
(has_hyponym)
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14466974-n:
congenital disorder characterized by high levels of cholesterol and early development of atherosclerosis
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Glosses
(gloss)
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05436752-n:
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
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Glosses
(gloss)
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14151139-n:
a disease or disorder that is inherited genetically
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