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MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 1
  • Multiple Birth Offspring - »õâ The offspring in multiple pregnancies (PREGNANCY, MULTIPLE): TWINS; TRIPLETS; QUADRUPLETS; QUINTUPLETS; etc.
    Synonyms : Multiple Birth, Multiple Births, Birth Offspring, Multiple, Birth, Multiple, Offspring, Multiple Birth, Sextuplet
  • Multiple Carboxylase Deficiency - »õâ A deficiency in the activities of biotin-dependent enzymes (propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, and PYRUVATE CARBOXYLASE) due to one of two defects in BIOTIN metabolism. The neonatal form is due to HOLOCARBOXYLASE SYNTHETASE DEFICIENCY. The late-onset form is due to BIOTINIDASE DEFICIENCY.
    Synonyms : Carboxylase Deficiency, Combined, Deficiency, Combined Carboxylase, Deficiency, Multiple Carboxylase, Carboxylase Deficiencies, Combined, Carboxylase Deficiencies, Multiple, Combined Carboxylase Deficiencies, Deficiencies, Combined Carboxylase
  • Multiple Chemical Sensitivity - »õâ An acquired disorder characterized by recurrent symptoms, referable to multiple organ systems, occurring in response to demonstrable exposure to many chemically unrelated compounds at doses below those established in the general population to cause harmful effects. (Cullen MR. The worker with multiple chemical sensitivities: an overview. Occup Med 1987;2(4):655-61)
    Synonyms : Chemical Sensitivities, Multiple, Chemical Sensitivity, Multiple, Idiopathic Environmental Intolerance, Multiple Chemical Sensitivities, Multiple Chemical Sensitivity Syndrome, Sensitivities, Multiple Chemical, Sensitivity, Multiple Chemical
  • Multiple Endocrine Neoplasia - »õâ A group of autosomal dominant diseases characterized by the combined occurrence of tumors involving two or more ENDOCRINE GLANDS that secrete PEPTIDE HORMONES or AMINES. These neoplasias are often benign but can be malignant. They are classified by the endocrine glands involved and the degree of aggressiveness. The two major forms are MEN1 and MEN2 with gene mutations on CHROMOSOME 11 and CHROMOSOME 10, respectively.
    Synonyms : Adenomatosis, Multiple Endocrine, Multiple Endocrine Adenopathy, Multiple Endocrine Neoplasia Syndromes, Multiple Endocrine Neoplasms, Adenomatoses, Familial Endocrine, Adenomatoses, Multiple Endocrine, Adenopathies, Multiple Endocrine
  • Multiple Endocrine Neoplasia Type 1 - »õâ A form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the PARATHYROID GLANDS, the PITUITARY GLAND, and the PANCREATIC ISLETS. The resulting clinical signs include HYPERPARATHYROIDISM; HYPERCALCEMIA; HYPERPROLACTINEMIA; CUSHING DISEASE; GASTRINOMA; and ZOLLINGER-ELLISON SYNDROME. This disease is due to loss-of-function of the MEN1 gene, a tumor suppressor gene (GENES, TUMOR SUPPRESSOR) on CHROMOSOME 11 (Locus: 11q13).
    Synonyms : MEA 1, MEA I, MEN I, MEN1, Multiple Endocrine Neoplasia Type I, Multiple Endocrine Neoplasms Type 1, Neoplasms, Multiple Endocrine Type I
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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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