Hyperonyms
(has_hyperonym)
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14151139-n:
a disease or disorder that is inherited genetically
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Hyponyms
(has_hyponym)
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14162563-n:
an autosomal recessive form of muscular dystrophy that appears anywhere from late childhood to middle age; characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle; usually progresses slowly with cardiopulmonary complications in the later stages
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Hyponyms
(has_hyponym)
|
14164007-n:
a disorder of lipid metabolism that is inherited as an autosomal recessive trait
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Hyponyms
(has_hyponym)
|
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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14169717-n:
a rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results
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Hyponyms
(has_hyponym)
|
14169897-n:
autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation
|
Hyponyms
(has_hyponym)
|
14170070-n:
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
|
Glosses
(gloss)
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00793988-a:
(of genes) producing its characteristic phenotype only when its allele is identical
|
Glosses
(gloss)
|
05439413-n:
a gene that has changed so that the normal transmission and expression of a trait is affected
|
Glosses
(gloss)
|
05443966-n:
any chromosome that is not a sex chromosome; appear in pairs in body cells but as single chromosomes in spermatozoa
|
Glosses
(gloss)
|
13957601-n:
the state of being present; current existence
|
Glosses
(gloss)
|
14070360-n:
an impairment of health or a condition of abnormal functioning
|
Glosses
(rgloss)
|
14169717-n:
a rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results
|
Glosses
(rgloss)
|
14169897-n:
autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation
|
Glosses
(rgloss)
|
14170070-n:
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
|
