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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • Chondro-4-Sulfatase - »õâ An enzyme from the sulfuric ester hydrolase class that breaks down one of the products of the chondroitin lyase II reaction. EC 3.1.6.9.
    Synonyms : Chondro 4 Sulfatase
  • Chondroblastoma - »õâ A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846)
    Synonyms : Chondroblastomas
  • Chondrocalcinosis - »õâ Presence of calcium salts, especially calcium pyrophosphate, in the cartilaginous structures of one or more joints. When accompanied by attacks of goutlike symptoms, it is called pseudogout. (Dorland, 27th ed)
    Synonyms : Chondrocalcinoses
  • Chondrocytes - »õâ Polymorphic cells that form cartilage.
    Synonyms : Chondroblast, Chondrocyte
  • Chondrodysplasia Punctata - »õâ A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.
    Synonyms : Hunermann-Conradi Syndrome, Conradi Hunermann Syndrome, Hunermann Conradi Syndrome, Syndrome, Conradi-Hunermann, Syndrome, Hunermann-Conradi
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MeSH(Medical Subject Headings) À¯»ç °Ë»ö (http://www.nlm.nih.gov) °á°ú : 0 ÆäÀÌÁö: 1
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