all items  in current results   Refine your search within these categories: 1. Human Genes (group results) 1-acylglycerol-3-phosphate O-acyltransferases [HGNC:AGPAT] (5) 5-HT (serotonin) receptors [HGNC:HTR] (18) 7TM orphan receptors [HGNC:O7TM] (2) A-kinase anchor proteins [HGNC:AKAP] (18) Abhydrolase domain containing [HGNC:ABHD] (8) Acetylcholine receptors, nicotinic [HGNC:CHRN] (19) Actin related protein 2/3 complex subunits [HGNC:ARPC] (2) Acyl-CoA synthetase family [HGNC:ACS] (11) Acyl-CoA thioesterases [HGNC:ACOT] (4) ADAM metallopeptidase domain containing [HGNC:ADAM] (7) more... 2. Interaction: Human Genes and Chemicals (group results) Affects (116) Decreases (119) Increases (121) 3. Bioactivity 4. Semantic Terms (group results) Entity [STY:T071] (26) A. 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Exceptions (129) C15. Hemic and Lymphatic Diseases (group results) Hematologic Diseases [MESH:D006402] (129) Lymphatic Diseases [MESH:D008206] (110) Z. Exceptions (46) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities: all > Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Urogenital Abnormalities [MESH:D014564] > Disorders of Sex Development [MESH:D012734] > Sex Chromosome Disorders of Sex Development [MESH:D058533] Freemartinism [MESH:D005611] (1) Gonadal Dysgenesis, Mixed [MESH:D006060] (1) Klinefelter Syndrome [MESH:D007713] (2) Male sterility due to Y-chromosome deletions [MESH:C536297] (1) Triple X syndrome [MESH:C535318] (1) Turner Syndrome [MESH:D014424] (131) C17. Skin and Connective Tissue Diseases (group results) Connective Tissue Diseases [MESH:D003240] (108) Skin Diseases [MESH:D012871] (121) C18. 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Wounds and Injuries (group results) Wounds and Injuries [MESH:D014947] (113) Z. Exceptions (92) D01. Inorganic Chemicals (group results) Arsenicals [MESH:D001152] (1) Cadmium Compounds [MESH:D019187] (1) Chlorine Compounds [MESH:D017606] (3) Electrolytes [MESH:D004573] (2) Elements [MESH:D004602] (7) Metals [MESH:D008670] (7) Nitrogen Compounds [MESH:D017672] (2) Sulfur Compounds [MESH:D013457] (1) Zinc Compounds [MESH:D017967] (1) D02. Organic Chemicals (group results) Organic Chemicals [MESH:D009930] (65) D03. Heterocyclic Compounds (group results) Heterocyclic Compounds [MESH:D006571] (29) D04. Polycyclic Compounds (group results) Polycyclic Compounds [MESH:D011083] (22) D05. Macromolecular Substances D06. Hormones, Hormone Substitutes, and Hormone Antagonists (group results) Hormones [MESH:D006728] (16) D08. Enzymes and Coenzymes (group results) Coenzymes [MESH:D003067] (1) D09. Carbohydrates (group results) Carbohydrates [MESH:D002241] (4) D10. 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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] > Urogenital Abnormalities [MESH:D014564] > Disorders of Sex Development [MESH:D012734] > Sex Chromosome Disorders of Sex Development [MESH:D058533] × 137 items, grouped by C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (view ungrouped items) Freemartinism [MESH:D005611] (1)    MESH:D005611   Freemartinism D005611               Gonadal Dysgenesis, Mixed [MESH:D006060] (1)    MESH:D006060   Gonadal Dysgenesis, Mixed D006060               Klinefelter Syndrome [MESH:D007713] (2)    MESH:D007713   Klinefelter Syndrome D007713               MESH:D013739   Testosterone D013739               Male sterility due to Y-chromosome deletions [MESH:C536297] (1)    MESH:C536297   Male sterility due to Y-chromosome deletions C536297               Triple X syndrome [MESH:C535318] (1)    MESH:C535318   Triple X syndrome C535318               Turner Syndrome [MESH:D014424] (131)    MESH:C004912   ethylbenzene C004912               MESH:C005095   malachite green C005095               MESH:C006253   pirinixic acid C006253               MESH:C006780   bisphenol A C006780               MESH:C009074   N-n-propylnorapomorphine C009074               MESH:C011512   alpha-naphthoflavone C011512               all 131 items...  (others) (1)    MESH:D058533   Sex Chromosome Disorders of Sex Development D058533