Related
(pertains_to)
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05443966-n:
any chromosome that is not a sex chromosome; appear in pairs in body cells but as single chromosomes in spermatozoa
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Related
(related_to)
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05443966-n:
any chromosome that is not a sex chromosome; appear in pairs in body cells but as single chromosomes in spermatozoa
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Glosses
(gloss)
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02676054-v:
be relevant to
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Glosses
(gloss)
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05443966-n:
any chromosome that is not a sex chromosome; appear in pairs in body cells but as single chromosomes in spermatozoa
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Glosses
(rgloss)
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14156134-n:
a genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth
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Glosses
(rgloss)
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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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Glosses
(rgloss)
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14161515-n:
a form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant
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Glosses
(rgloss)
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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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Glosses
(rgloss)
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14163182-n:
a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
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Glosses
(rgloss)
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14163676-n:
a form of muscular dystrophy that usually begins between early adulthood and middle age and first affects muscles of the eyelid and throat; progresses slowly with swallowing problems common as the disease progresses; inheritance is autosomal dominant
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Glosses
(rgloss)
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14164007-n:
a disorder of lipid metabolism that is inherited as an autosomal recessive trait
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Glosses
(rgloss)
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14171176-n:
a form of hemophilia discovered by Erik von Willebrand; a genetic disorder that is inherited as an autosomal recessive trait; characterized by a deficiency of the coagulation factor and by mucosal bleeding
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Glosses
(rgloss)
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14537735-n:
a rare genetic condition characterized by an eruption of exposed skin occurring in childhood and photosensitivity with severe sunburn; inherited as a recessive autosomal trait in which DNA repair processes are defective so they are more likely to chromosome breaks and cancers when exposed to ultraviolet light
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