| Eponyms in category: Endocrine |
| 36
main and alternative
entries found.
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| Addison's disease |
| Disease resulting from progressive destruction of the adrenal gland with deficiency in the secretion of adreno-cortical hormones. |
| Addison’s melanoderma (Addison's disease) |
| Disease resulting from progressive destruction of the adrenal gland with deficiency in the secretion of adreno-cortical hormones. |
| Addison’s syndrome (Addison's disease) |
| Disease resulting from progressive destruction of the adrenal gland with deficiency in the secretion of adreno-cortical hormones. |
| Basedow's syndrome or disease |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Begbie's disease (Basedow's syndrome or disease) |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Elephant man's syndrome (misnomer) (Recklinghausen's disease) |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| Flajani's disease (Basedow's syndrome or disease) |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Flajani-Basedow syndrome (Basedow's syndrome or disease) |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Graves' disease (Basedow's syndrome or disease) |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Kaposi's disease I |
| A skin disease marked by numerous whitish punctiform papules and brownish macules arranged in a necklacelike pattern. |
| Klinefelter's syndrome |
| A congenital endocrine disturbance characterized chiefly by dull mentality and/or behavioural problems associated with hypogenitalism and hypogonadism. |
| Klinefelter-Reifenstein syndrome (Klinefelter's syndrome) |
| A congenital endocrine disturbance characterized chiefly by dull mentality and/or behavioural problems associated with hypogenitalism and hypogonadism. |
| Klinefelter-Reifenstein-Albright syndrome (Klinefelter's syndrome) |
| A congenital endocrine disturbance characterized chiefly by dull mentality and/or behavioural problems associated with hypogenitalism and hypogonadism. |
| Leydig cell deficiency syndrome (Wilkins-Bergada syndrome) |
| A syndrome of small gonads either in the scrotum or inguinal channel, small penis and hypospadias. |
| Marie's disease |
| A rare chronic condition, usually caused by an adenoma. It is characterized by hyperfunction of the anterior pituitary gland associated with hypersecretion of growth hormone, resulting in enlargement of bones and soft tissue of hands, feet, and face. |
| Marie's syndrome II (Marie's disease) |
| A rare chronic condition, usually caused by an adenoma. It is characterized by hyperfunction of the anterior pituitary gland associated with hypersecretion of growth hormone, resulting in enlargement of bones and soft tissue of hands, feet, and face. |
| Marsh's disease (Basedow's syndrome or disease) |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Morgagni-Shereshevskii-Turner-Albright syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Morgagni-Turner syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Morgagni-Turner-Albright syndrome |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Parry's disease (Basedow's syndrome or disease) |
| A disorder characterized by a triad of hyperthyroidism, goiter, and exophthalmos (bulging eyeballs). |
| Pierre Marie disease (Marie's disease) |
| A rare chronic condition, usually caused by an adenoma. It is characterized by hyperfunction of the anterior pituitary gland associated with hypersecretion of growth hormone, resulting in enlargement of bones and soft tissue of hands, feet, and face. |
| Recklinghausen syndrome (Recklinghausen's disease) |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| Recklinghausen's disease |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| Recklinghausen's phakomatosis (Recklinghausen's disease) |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| Recklinhausen neurofibromatosis (Recklinghausen's disease) |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| Reifenstein-Albright XXY syndrome (Klinefelter's syndrome) |
| A congenital endocrine disturbance characterized chiefly by dull mentality and/or behavioural problems associated with hypogenitalism and hypogonadism. |
| Schereshevskii-Turner syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Turner's syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Turner-Albright syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Turner-Vary syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| Ullrich-Turner syndrome (Morgagni-Turner-Albright syndrome) |
| Congenital endocrine disorder with short stature, absence of secondary sexual characteristics, failure of sexual maturation, webbing of the neck and inconsistent cardiac defects. |
| von Recklinghausen neuropathy (Recklinghausen's disease) |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| von Recklinghausen's disease (Recklinghausen's disease) |
| Inheritable disease characterized by café au lait spots combined with multiple peripheral nerve tumours and a variety of others dysplastic abnormalities of the skin, nervous system, bones, endocrine organs and blood vessels. |
| Wilkins-Bergada syndrome |
| A syndrome of small gonads either in the scrotum or inguinal channel, small penis and hypospadias. |
| Wise-Rein disease (Kaposi's disease I) |
| A skin disease marked by numerous whitish punctiform papules and brownish macules arranged in a necklacelike pattern. |
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