| COACH | cerebellar vermis hypoplasia/aplasia-oligophrenia-congenital ataxia-ocular colobomata-hepatic fibros... |
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| PPA | palpation, percussion, auscultation; pepsin A; phenylpropanolamine; phenylpyruvic acid; Pittsburgh p... |
| cataract-oligophrenia syndrome | <syndrome> A rare neurologic disorder characterised by cerebellolental degeneration with mental retardation; autosomal recessive inheritance. Synonym: cataract-oligophrenia syndrome, Marinesco-Sjogren syndrome, Torsten Sjogren's syndrome. (05 Mar 2000) |
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| phenylpyruvate oligophrenia | <disease> Congenital absence of phenylalanine hydroxylase (an enzyme that converts phenylalanine into tyrosine). Phenylalanine accumulates in blood and seriously impairs early neuronal development. The defect can be controlled by diet and is not serious if treated in this way. Incidence: highest in Caucasians. Acronym: PKU Origin: Gr. Ouron = urine (15 Oct 1997) |
| phenylpyruvic acid | C6H5-CH2COCOOH;the transaminated product of the action of phenylalanine aminotransferase; elevated in the urine in individuals with phenylketonuria. (05 Mar 2000) |
| phenylpyruvic acids | A group of compounds that are derivatives of phenylpyruvic acid which has the general formula c6h5ch2cocooh, and is a metabolite of phenylalanine. (12 Dec 1998) |
| phenylpyruvic amentia | Amentia accompanied by the appearance of phenylpyruvate in the urine. (05 Mar 2000) |
| oligophrenia | Synonym: mental retardation. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|