| » Hageman Factor Deficiency
Hageman Factor Deficiency is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s)...
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| » Hemangioma Thrombocytopenia Syndrome
Hemangioma-Thrombocytopenia Syndrome (also known as Kasabach-Merritt Syndrome) is a rare disorder characterized by an abnormal
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| » Hyperhidrosis, Primary
Primary Hyperhidrosis is a rare disorder characterized by excessive activity (hyperactivity) of the sweat glands (eccrine)
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| » Hypophosphatasia
Hypophosphatasia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision
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| » Hyperoxaluria, Primary (Type I)
Primary Hyperoxaluria (Type I) is a hereditary disorder characterized by an inborn error of glyoxylate.
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| » Hypotonia, Benign Congenital
Benign congenital hypotonia (BCH) has been an outdated term since 1956, when the first congenital muscle disease, central core disease, was describ...
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| » Heart Attack and Unstable Angina
A heart attack occurs when one or more of the coronary arteries is blocked, depriving heart muscle of oxygen-rich blood. Without blood supply, the ...
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| » Tension Headaches
A tension headache causes constant, steady ache and tightness around your forehead, both temples, or back of your head and neck.
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| » Head Injury, Age 3 and Younger
Almost all children will injure their heads, especially when they are babies or toddlers and are just learning to roll over, crawl, or walk. These ...
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| » Hajdu Cheney Syndrome
Hajdu-Cheney Syndrome is a rare connective tissue disorder. Connective tissue is strong fibrous tissue that supports and joins other body tissues a...
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| » Hypochondroplasia
Hypochrondroplasia is a genetic disorder characterized by small stature and disproportionately short arms, legs, hands, and feet (short-limbed dwar...
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| » Hemoglobinuria, Paroxysmal Cold
It is possible that the main title of the report Hemoglobinuria, Paroxysmal Cold is not the name you expected. Please check the synonyms listing to...
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| » Hallermann Streiff syndrome
Hallermann-Streiff syndrome is a rare genetic disorder that is primarily characterized by distinctive malformations of the skull and facial (cranio...
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| » Hanhart Syndrome
Hanhart Syndrome is a rare birth defect that is characterized by a short, incompletely developed tongue
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| » Hyperprolinemia Type II
Two types of hyperprolinemia are recognized by physicians and clinical researchers. Each represents an inherited inborn error of metabolism involvi...
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| » Hyperostosis Frontalis Interna
Hyperostosis Frontalis Interna is characterized by the thickening of the frontal bone of the skull. It is not clear that this disorder is actually ...
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| » Hypoglycemia
Hypoglycemia is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by t...
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