| DBP | diastolic blood pressure; dibutylphthalate; distobuccopulpal; Dohle body panmyelopathy; vitamin D-bi... |
|---|---|
| CAA | carotid audiofrequency analysis; cerebral amyloid angiopathy; circulating anodic antigen; Clean Air ... |
| CCA | cephalin cholesterol antigen; chick cell agglutination; chimpanzee coryza agent; choriocarcinoma; ci... |
| CHD | Chediak-Higashi disease; childhood disease; chronic hemodialysis; congenital or congestive heart dis... |
| CPI | California Personality Inventory; Cancer Potential Index; congenital palatopharyngeal incompetence; ... |
| CDGP | Constitutional delay of growth and puberty |
|---|---|
| LOH | Loss of constitutional heterozygosity |
| CGD | constitutional growth delay |
| CSS | constitutional short stature |
| EIEE | Early infantile epileptic encephalopathy |
| constitutional | 1. Affecting the whole constitution of the body, not local. 2. Pertaining to the constitution. (18 Nov 1997) |
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| constitutional cause | A cause acting from within or through some systemic process or inborn error. (05 Mar 2000) |
| constitutional formula | A formula in which the connections of the atoms and groups of atoms, as well as their kind and number, are indicated. Synonym: constitutional formula, graphic formula. (05 Mar 2000) |
| constitutional hepatic dysfunction | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| constitutional hirsutism | Mild to moderate degree of hirsutism present in an individual exhibiting otherwise normal endocrine and reproductive function. (05 Mar 2000) |
| constitutional liver dysfunction | An inherited disorder that affects the way bilirubin in handled by the liver. Thought to be due to an inborn error of bilirubin metabolism. Symptoms include mild jaundice, weakness, fatigue, nausea and abdominal pain. (27 Sep 1997) |
| constitutional psychology | The psychology of the individual as related to body habitus. (05 Mar 2000) |
| constitutional reaction | A generalised reaction in contrast to a focal or local reaction; in allergy the immediate or delayed response, following the introduction of an allergen, occurring at sites remote from that of injection. (05 Mar 2000) |
| constitutional symptom | A symptom indicating a systemic effect of a disease; e.g., weight loss. (05 Mar 2000) |
| constitutional thrombopathy | <haematology> A form of congenital platelet functional defect that result in prolongation of the bleeding time. Characteristics include mucosal and post-operative bleeding that may be severe. (17 Dec 1997) |
| constitutional ulcer | An ulcer due to systemic disease, such as tuberculosis. Synonym: symptomatic ulcer. (05 Mar 2000) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| autism, infantile | A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment. (12 Dec 1998) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| spasms, infantile | Primary generalised epileptic seizures occurring in infants between birth and twelve months of age consisting of brief synchronous contractions of the neck, torso, and both arms. These seizures often occur in infants with underlying neurologic diseases. The prognosis for these infants is grave, with approximately ninety percent developing mental retardation in addition to their seizures. The eeg has a typical hypsarrhythmia pattern. The spasms and hypsarrhythmia have a tendency to disappear over the first three to five years of life, only to be replaced by other forms of generalised seizures. Infantile spasms sometimes respond to valproic acid or acth. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|