| Eponyms in category: Metabolism and metabolic disturbances |
| 68
main and alternative
entries found.
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| Addison disease-cerebral sclerosis syndrome (Addison-Schilder syndrome) |
| A metabolic disorder combining the characteristics of Addison’s disease (bronze skin disease) and cerebral sclerosis (Schilder disease). |
| Addison-Schilder syndrome |
| A metabolic disorder combining the characteristics of Addison’s disease (bronze skin disease) and cerebral sclerosis (Schilder disease). |
| Albright-Butler-Bloomberg disease |
| A metabolic syndrome marked by dwarfism and other severe developmental anomalies. |
| Albright-Butler-Bloomberg syndrome (Albright-Butler-Bloomberg disease) |
| A metabolic syndrome marked by dwarfism and other severe developmental anomalies. |
| Alder's anomaly (Alder-Reilly anomaly) |
| Inheritable anomaly with disturbance of the polysaccharid metabolism. |
| Alder's syndrome (Alder-Reilly anomaly) |
| Inheritable anomaly with disturbance of the polysaccharid metabolism. |
| Alder-Reilly anomaly |
| Inheritable anomaly with disturbance of the polysaccharid metabolism. |
| Aub-Dubois table |
| Table of normal basal metabolic rates.
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| Béguez César's syndrome |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Beguez César-Steinbrinck-Chédiak-Higashi syndrome (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Chédiak's anomaly (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Chédiak's disease (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Chédiak-Higashi syndrome (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Chédiak-Steinbrinck syndrome (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Chédiak-Steinbrinck-Higashi syndrome (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Cori cycle |
| Phases in the metabolism of carbohydrate. |
| Cori’s type VI glycogenosis (Hers' disease) |
| An inborn glycogen metabolism disorder caused by deficiency of hepatic phosphorylase, associated with an enlarged liver and mild hypoglycaemia. |
| Crocker's syndrome (Niemann-Pick disease (Ludwig Pick)) |
| A disturbance of sphingolipid metabolism characterised by enlargement of liver and spleen, anaemia, cherry red spot of the macula with progressive blindness, lymphadenopathy, and progressive mental and physical deterioration. |
| Crocker-Farber syndrome (Niemann-Pick disease (Ludwig Pick)) |
| A disturbance of sphingolipid metabolism characterised by enlargement of liver and spleen, anaemia, cherry red spot of the macula with progressive blindness, lymphadenopathy, and progressive mental and physical deterioration. |
| De Crecchio's syndrome (Fibiger-Debré von Gierke syndrome) |
| Adrenogenital syndrome of salt loss. An inborn error of metabolism characterized by a deficiency of enzymes involved in the production of adrenocorticosteroid hormones. |
| Fanconi-Prader syndrome (Addison-Schilder syndrome) |
| A metabolic disorder combining the characteristics of Addison’s disease (bronze skin disease) and cerebral sclerosis (Schilder disease). |
| Farber's disease |
| Rare, inheritable, disturbance of the fatty metabolism induced by a lysosomal enzyme deficiency with accumulation of ceramide in the tissues. |
| Farber-Uzman syndrome (Farber's disease) |
| Rare, inheritable, disturbance of the fatty metabolism induced by a lysosomal enzyme deficiency with accumulation of ceramide in the tissues. |
| Farber’s lipogranulomatosis (Farber's disease) |
| Rare, inheritable, disturbance of the fatty metabolism induced by a lysosomal enzyme deficiency with accumulation of ceramide in the tissues. |
| Fibiger-Debré syndrome (Fibiger-Debré von Gierke syndrome) |
| Adrenogenital syndrome of salt loss. An inborn error of metabolism characterized by a deficiency of enzymes involved in the production of adrenocorticosteroid hormones. |
| Fibiger-Debré von Gierke syndrome |
| Adrenogenital syndrome of salt loss. An inborn error of metabolism characterized by a deficiency of enzymes involved in the production of adrenocorticosteroid hormones. |
| Følling's disease |
| An inborn error of metabolism in which the body lacks the ability to break down the amino acid fenylananin in the blood, causing severe mental deficiency. |
| Følling's syndrome (Følling's disease) |
| An inborn error of metabolism in which the body lacks the ability to break down the amino acid fenylananin in the blood, causing severe mental deficiency. |
| Gallais' syndrome (Fibiger-Debré von Gierke syndrome) |
| Adrenogenital syndrome of salt loss. An inborn error of metabolism characterized by a deficiency of enzymes involved in the production of adrenocorticosteroid hormones. |
| Hers' disease |
| An inborn glycogen metabolism disorder caused by deficiency of hepatic phosphorylase, associated with an enlarged liver and mild hypoglycaemia. |
| Hers' syndrome (Hers' disease) |
| An inborn glycogen metabolism disorder caused by deficiency of hepatic phosphorylase, associated with an enlarged liver and mild hypoglycaemia. |
| Hunter’s syndrome (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Hurler's disease (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Hurler's syndrome |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Hurler's variant |
| An inborn error of metabolism with features similar to a mild form of the Hurler syndrome. |
| Hurler-Hunter syndrome (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Hurler-Pfaundler syndrome (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Hurler-Scheie syndrome |
| A metabolic syndrome combining symptoms less severe than Hurler’s syndrome, more severe than Scheie’s syndrome. |
| Johnie McL disease (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Kinnier Wilson's disease (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Maroeteaux-Lamy syndrome I |
| An uncommon disorder of mucopolysaccharide marked by dwarfism, hearing loss, and progressive skeletal deformity, etc. |
| Niemann's disease (Niemann-Pick disease (Ludwig Pick)) |
| A disturbance of sphingolipid metabolism characterised by enlargement of liver and spleen, anaemia, cherry red spot of the macula with progressive blindness, lymphadenopathy, and progressive mental and physical deterioration. |
| Niemann-Pick disease (Ludwig Pick) |
| A disturbance of sphingolipid metabolism characterised by enlargement of liver and spleen, anaemia, cherry red spot of the macula with progressive blindness, lymphadenopathy, and progressive mental and physical deterioration. |
| Pfaundler-Hurler disease (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Pfaundler-Hurler syndrome (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Pick's disease (Ludwig Pick) (Niemann-Pick disease (Ludwig Pick)) |
| A disturbance of sphingolipid metabolism characterised by enlargement of liver and spleen, anaemia, cherry red spot of the macula with progressive blindness, lymphadenopathy, and progressive mental and physical deterioration. |
| Pirie’s syndrome (Fibiger-Debré von Gierke syndrome) |
| Adrenogenital syndrome of salt loss. An inborn error of metabolism characterized by a deficiency of enzymes involved in the production of adrenocorticosteroid hormones. |
| Reilly's anomaly (Alder-Reilly anomaly) |
| Inheritable anomaly with disturbance of the polysaccharid metabolism. |
| Reilly's granulation anomaly (Alder-Reilly anomaly) |
| Inheritable anomaly with disturbance of the polysaccharid metabolism. |
| Schilder-Addison syndrome (Addison-Schilder syndrome) |
| A metabolic disorder combining the characteristics of Addison’s disease (bronze skin disease) and cerebral sclerosis (Schilder disease). |
| Schilder’s disease (Addison-Schilder syndrome) |
| A metabolic disorder combining the characteristics of Addison’s disease (bronze skin disease) and cerebral sclerosis (Schilder disease). |
| Sheldon-Ellis syndrome (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Sidbury's syndrome |
| Rare inheritable defect of leucine metabolism causing a urinous odour from sweaty feet, |
| Sidbury-Harlan-Wittels syndrome (Sidbury's syndrome) |
| Rare inheritable defect of leucine metabolism causing a urinous odour from sweaty feet, |
| Sidbury-Smith-Harlan syndrome (Sidbury's syndrome) |
| Rare inheritable defect of leucine metabolism causing a urinous odour from sweaty feet, |
| Siemerling-Creutzfeldt syndrome (Addison-Schilder syndrome) |
| A metabolic disorder combining the characteristics of Addison’s disease (bronze skin disease) and cerebral sclerosis (Schilder disease). |
| Steinbrinck Granulationsanomalie (German) (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Steinbrinck's anomaly (Béguez César's syndrome) |
| A multisystem fatal familial metabolic disorder with abnormal granulation of leukocytes and susceptibility to infections. |
| Thiébaut's syndrome (Van Bogaert-Scherer-Epstein syndrome) |
| A familial disorder of metabolism. |
| Thompson’s syndrome (Hurler's syndrome) |
| A metabolical disease characterized by dwarfism, hunchback, gargoyle like facies, mental retardation, and a large number of other abnormalities. |
| Van Bogaert-Scherer-Epstein syndrome |
| A familial disorder of metabolism. |
| Westphal's pseudosclerosis (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Westphal-Strümpell disease (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Westphal-Strümpell pseudosclerosis (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Westphal-Strümpell syndrome (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Wilkins' disease (Fibiger-Debré von Gierke syndrome) |
| Adrenogenital syndrome of salt loss. An inborn error of metabolism characterized by a deficiency of enzymes involved in the production of adrenocorticosteroid hormones. |
| Wilson's disease |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
| Wilson-Konovalov disease (Wilson's disease) |
| A chronic disease of brain and liver with progressive neurological dysfunction, due to a disturbance of copper metabolism. |
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