- autosomal recessive prolidase deficiency
- 常染色体隐性遗传氨酰脯基氨酸<二肽>酶缺乏
Medical Chinese dictionary (湘雅医学词典). 2013.
autosomal recessive prolidase deficiency
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Prolidase deficiency — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29838 ICD10 = ICD9 = ICDO = OMIM = 170100 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Prolidase deficiency is a rare autosomal recessive [cite journal |pmid=7187192 |year=1982… … Wikipedia
prolidase deficiency — pro·li·dase de·fi·cien·cy (proґlĭ dās) an autosomal recessive aminoacidopathy due to mutation in the PEPD gene (locus: 19cen q13.11), which encodes X Pro dipeptidase; defective cleavage of imidodipeptides results in imidodipeptiduria.… … Medical dictionary
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