| ¿µ¹® | hypoparathyroidism | ÇÑ±Û | ºÎ°©»ó»ù±â´ÉÀúÇÏÁõ |
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| IHP | idiopathic hypoparathyroidism; idiopathic hypopituitarism; individualized health plan; inositol hexa... |
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| IPH | idiopathic portal hypertension; idiopathic pulmonary hemosiderosis; idiopathic pulmonary hypertensio... |
| HSM Syndrome | juvenile-familial Endocrinopathy Hypoparathyroidism Addison's Disease Menillansis |
| FIH | familial isolated hypoparathyroidism; fat-induced hyperglycemia |
| HAM | hearing aid microphone; helical axis in motion; human albumin microsphere; human alveolar macrophage... |
| IHP | idiopathic hypoparathyroidism |
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| PHP | Pseudo-hypoparathyroidism |
| AISA | Acquired Idiopathic Sideroblastic Anemia |
| AIS | Adolescent Idiopathic Scoliosis |
| CIU | Chronic Idiopathic Urticaria |
| idiopathic hypoparathyroidism | <radiology> Rare condition of unknown cause, round face; short dwarf-like; obese, mental retardation, cataracts, dry scaly skin; atrophy of nails, dental hypoplasia (delayed tooth eruption, impaction of teeth, supernumerary teeth) see: hypoparathyroidism (12 Dec 1998) |
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| hypoparathyroidism | <endocrinology> A term which describes the abnormally low production of parathyroid hormone by the parathyroid glands. Hypoparathyroidism may be congenital or occur in association with another disorder (autoimmune disease, haemochromatosis). Common symptoms are those of low blood calcium: muscle spasms, tetany, facial grimacing, laryngeal spasm and seizures. (11 Jan 1998) |
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| hypoparathyroidism syndrome | <syndrome> A syndrome characterised by fatigue, muscular weakness, paresthesia and cramps of the extremities, tetany, and laryngeal stridor; due to hypocalcaemia resulting from a lack of parathyroid hormone; may be idiopathic, postoperative, or caused by organic lesions of the parathyroids. (05 Mar 2000) |
| immunodeficiency with hypoparathyroidism | diGeorge syndrome |
| acute idiopathic polyneuritis | <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin. The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months. Synonym: Guillain-Barre syndrome (12 Jul 2000) |
| chronic idiopathic jaundice | <syndrome> An inherited disorder (autosomal recessive) that is characterised by long-standing mild jaundice. This occurs secondary to an abnormality in the transport of bilirubin from the liver to the biliary system. This leads to an accumulation of bilirubin in the liver. Avoidance of alcohol and medications which can affect the liver is important. Inheritance: autosomal recessive. (27 Sep 1997) |
| chronic idiopathic xanthomatosis | Vague or indefinite term for inherited abnormalities of lipid metabolism leading to xanthoma formation (e.g., primary familial xanthomatosis). (05 Mar 2000) |
| multiple idiopathic haemorrhagic sarcoma | <oncology, tumour> A type of vascular cancer characterised by soft purple nodules that usually develop first on the feet and then slowly spread across the skin.This cancer is most often found in people with compromised immune systems, such as AIDS patients. (09 Oct 1997) |
| primary idiopathic macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| purpura, thrombocytopenic, idiopathic | Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IgG autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. (12 Dec 1998) |
| hyperostosis, diffuse idiopathic skeletal | A disease of elderly men characterised by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions. (12 Dec 1998) |
| diffuse idiopathic skeletal hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| idiopathic | Of the nature of an idiopathy, self originated, of unknown causation. (18 Nov 1997) |
| idiopathic aldosteronism | An adrenocortical disorder caused by excessive secretion of aldosterone and characterised by headaches, nocturia, polyuria, fatigue, hypertension, potassium depletion, hypokalaemic alkalosis, hypervolaemia, and decreased plasma renin activity; may be associated with small benign adrenocortical adenomas. Synonym: Conn's syndrome, idiopathic aldosteronism. (05 Mar 2000) |
| idiopathic bilateral vestibulopathy | Slowly progressive disorder affecting young to middle-aged adults, manifested as gait unsteadiness (especially when visual cues are absent) and oscillopsia, unaccompanied by vertigo and hearing loss. (05 Mar 2000) |
| idiopathic bone cavity | A unilocular cyst containing serous fluid and lined with a thin layer of connective tissue, occurring usually in the shaft of a long bone in a child. Synonym: idiopathic bone cavity, osteocystoma, simple bone cyst, traumatic bone cyst, unicameral bone cyst. (05 Mar 2000) |
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