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C13. Female Urogenital Diseases and Pregnancy Complications (group results) |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (group results) |
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C18. Nutritional and Metabolic Diseases: all > Metabolic Diseases [MESH:D008659] > Glucose Metabolism Disorders [MESH:D044882] > Hypoglycemia [MESH:D007003] |
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency [MESH:C567784] (102)
ACTH Deficiency, Isolated [MESH:C562707] (124)
Carnitine palmitoyl transferase 1A deficiency [MESH:C535588] (133)
Carnitine Palmitoyltransferase II Deficiency, Infantile [MESH:C563462] (52)
Congenital Hyperinsulinism [MESH:D044903] (132)
Hyperinsulinemic hypoglycemia, familial, 3 [MESH:C538374] (82)
Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)
Hyperinsulinemic Hypoglycemia, Familial, 5 [MESH:C566494] (94)
Hyperinsulinemic hypoglycemia, familial, 6 [MESH:C538375] (64)
Hyperinsulinemic hypoglycemia, familial, 7 [MESH:C538376] (106)
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D06. Hormones, Hormone Substitutes, and Hormone Antagonists (group results) |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment (group results) |
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I. Anthropology, Education, Sociology and Social Phenomena |
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