all items  in current results   Refine your search within these categories: 1. Human Genes (group results) Cytochrome P450s [HGNC:CYP] (1) Nuclear hormone receptors [HGNC:NR] (1) 2. Interaction: Human Genes and Chemicals (group results) Affects (1) Decreases (1) Increases (1) 3. Bioactivity 4. Semantic Terms A. Anatomy (group results) Cells [MESH:D002477] (1) B. Organisms C01. Bacterial Infections and Mycoses (group results) Infection [MESH:D007239] (1) C02. Virus Diseases C03. Parasitic Diseases C04. Neoplasms (group results) Neoplasms [MESH:D009369] (1) C05. Musculoskeletal Diseases (group results) Musculoskeletal Diseases [MESH:D009140] (1) C06. Digestive System Diseases (group results) Digestive System Diseases [MESH:D004066] (1) C07. Stomatognathic Diseases C08. Respiratory Tract Diseases (group results) Respiratory Tract Diseases [MESH:D012140] (1) C09. Otorhinolaryngologic Diseases C10. Nervous System Diseases (group results) Nervous System Diseases [MESH:D009422] (3) Z. Exceptions (1) C11. Eye Diseases (group results) Eye Diseases [MESH:D005128] (3) C12. Male Urogenital Diseases (group results) Male Urogenital Diseases [MESH:D052801] (1) C13. Female Urogenital Diseases and Pregnancy Complications (group results) Female Urogenital Diseases [MESH:D052776] (1) C14. Cardiovascular Diseases (group results) Cardiovascular Diseases [MESH:D002318] (1) Z. Exceptions (1) C15. Hemic and Lymphatic Diseases (group results) Hematologic Diseases [MESH:D006402] (1) Lymphatic Diseases [MESH:D008206] (1) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Nervous System Malformations [MESH:D009421] > Agenesis of Corpus Callosum [MESH:D061085] > Aicardi Syndrome [MESH:D058540] X-linked infantile spasm syndrome [MESH:C538670] (1) C17. Skin and Connective Tissue Diseases (group results) Skin Diseases [MESH:D012871] (1) C18. Nutritional and Metabolic Diseases (group results) Metabolic Diseases [MESH:D008659] (1) Nutrition Disorders [MESH:D009748] (1) Z. Exceptions (1) C19. Endocrine System Diseases (group results) Endocrine System Diseases [MESH:D004700] (1) C20. Immune System Diseases (group results) Immune System Diseases [MESH:D007154] (1) C21. Disorders of Environmental Origin C22. Animal Diseases C23. Pathological Conditions, Signs and Symptoms (group results) Pathologic Processes [MESH:D010335] (1) Pathological Conditions, Anatomical [MESH:D020763] (1) Signs and Symptoms [MESH:D012816] (1) C24. Occupational Diseases C25. Chemically-Induced Disorders (group results) Substance-Related Disorders [MESH:D019966] (1) C26. Wounds and Injuries (group results) Wounds and Injuries [MESH:D014947] (1) Z. Exceptions (1) D01. Inorganic Chemicals D02. Organic Chemicals D03. Heterocyclic Compounds D04. Polycyclic Compounds D05. Macromolecular Substances D06. Hormones, Hormone Substitutes, and Hormone Antagonists (group results) Hormones [MESH:D006728] (1) D08. Enzymes and Coenzymes D09. Carbohydrates D10. Lipids D12. Amino Acids, Peptides, and Proteins (group results) Peptides [MESH:D010455] (1) Proteins [MESH:D011506] (1) D13. Nucleic Acids, Nucleotides, and Nucleosides D20. Complex Mixtures D23. Biological Factors D25. Biomedical and Dental Materials D26. Pharmaceutical Preparations D27. Chemical Actions and Uses E. Analytical, Diagnostic and Therapeutic Techniques and Equipment F. Psychiatry and Psychology (group results) Mental Disorders [MESH:D001523] (1) G. Phenomena and Processes (group results) Genetic Phenomena [MESH:D055614] (1) I. Anthropology, Education, Sociology and Social Phenomena J. Technology, Industry, Agriculture N. Health Care Recently Viewed Items Go to Item History

These terms define your current search. Click the × to remove a term. C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Nervous System Malformations [MESH:D009421] > Agenesis of Corpus Callosum [MESH:D061085] > Aicardi Syndrome [MESH:D058540] × 3 results Group by: C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities Sort by: MeSH_UID, MeSH_NAME   MESH:C538670   X-linked infantile spasm syndrome C538670               MESH:D000324   Adrenocorticotropic Hormone D000324               MESH:D058540   Aicardi Syndrome D058540