Hyperonyms
(has_hyperonym)
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14204950-n:
any deviation from a healthy or normal condition
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Hyponyms
(has_hyponym)
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14207256-n:
inherited form of hemochromatosis
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Hyponyms
(has_hyponym)
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14207388-n:
hemochromatosis resulting from repeated transfusions or from excessive intake of foods containing iron
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Glosses
(gloss)
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00158804-v:
collect or gather
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Glosses
(gloss)
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00244958-a:
(of skin) having a tan color from exposure to the sun
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Glosses
(gloss)
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01176695-a:
larger than normal
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Glosses
(gloss)
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05238282-n:
a natural protective body covering and site of the sense of touch
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Glosses
(gloss)
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05267345-n:
part of an organism consisting of an aggregate of cells having a similar structure and function
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Glosses
(gloss)
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05385534-n:
large and complicated reddish-brown glandular organ located in the upper right portion of the abdominal cavity; secretes bile and functions in metabolism of protein and carbohydrate and fat; synthesizes substances involved in the clotting of the blood; synthesizes vitamin A; detoxifies poisonous substances and breaks down worn-out erythrocytes
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Glosses
(gloss)
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05387167-n:
a large elongated exocrine gland located behind the stomach; secretes pancreatic juice and insulin
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Glosses
(gloss)
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05595083-n:
(anatomy) the point of connection between two bones or elements of a skeleton (especially if it allows motion)
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Glosses
(gloss)
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14118138-n:
diabetes caused by a relative or absolute deficiency of insulin and characterized by polyuria
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Glosses
(gloss)
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14204950-n:
any deviation from a healthy or normal condition
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Glosses
(gloss)
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14642417-n:
a heavy ductile magnetic metallic element; is silver-white in pure form but readily rusts; used in construction and tools and armament; plays a role in the transport of oxygen by the blood
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Glosses
(rgloss)
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00698609-n:
surgical incision into a vein; used to treat hemochromatosis
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Glosses
(rgloss)
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14207256-n:
inherited form of hemochromatosis
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Glosses
(rgloss)
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14207388-n:
hemochromatosis resulting from repeated transfusions or from excessive intake of foods containing iron
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Glosses
(rgloss)
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14314597-n:
abnormal deposit of hemosiderin; often a symptom of thalassemia or hemochromatosis
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