Item 2 of 16 (back to results) previous next   16 alpha-ethyl-21-hydroxy-19-nor-4-pregnene-3,20-dione C020175               MeSH Unique Identifier: C020175 Chemical – Gene Interaction Note 1: 16 alpha-ethyl-21-hydroxy-19-nor-4-pregnene-3,20-dione results in decreased expression of AHNAK2 mRNA Note 2: 16 alpha-ethyl-21-hydroxy-19-nor-4-pregnene-3,20-dione results in increased expression of AKAP13 mRNA Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Musculoskeletal Abnormalities [MESH:D009139] > Limb Deformities, Congenital [MESH:D017880] > Upper Extremity Deformities, Congenital [MESH:D038062] > Hand Deformities, Congenital [MESH:D006228] > Schinzel-Giedion syndrome [MESH:C536632] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  A-kinase anchor proteins [HGNC:AKAP] (99)   A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)  Basic leucine zipper proteins [HGNC:bZIP] (670)   CCAAT/enhancer binding protein (C/EBP), delta [HGNC:CEBPD] (51)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566)  Laminins [HGNC:LAM] (93)   laminin, gamma 1 (formerly LAMB2) [HGNC:LAMC1] (29)  Neuropeptide receptors [HGNC:NPR] (30)   Neuropeptide S receptors [HGNC:NPSR] (22)   neuropeptide Y receptor Y1 [HGNC:NPY1R] (18)  Nuclear hormone receptors [HGNC:NR] (1322)   progesterone receptor [HGNC:PGR] (209)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)  Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105)   A kinase (PRKA) anchor protein 13 [HGNC:AKAP13] (18)  Short chain dehydrogenase/reductase superfamily [HGNC:SDR] (302)   Short chain dehydrogenase/reductase superfamily, Classical fold cluster 2 [HGNC:SDRC2] (140)   hydroxysteroid (11-beta) dehydrogenase 02 [HGNC:HSD11B2] (72) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   binding (2423)  cotreatment (1499)  localization (731)  Decreases (5154)   expression (2187)  reaction (3393)  Increases (5571)   activity (2865)  expression (3238)  reaction (1574)  response to substance (641) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   RNA Virus Infections [MESH:D012327] (4215)   Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Hamartoma [MESH:D006222] (1484)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myeloid, Acute [MESH:D015470] (2176)  Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative [MESH:D054438] (18)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Carcinoma [MESH:D002277] (7263)   Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Meningioma [MESH:D008579] (978)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Head and Neck Neoplasms [MESH:D006258] (4612)   Mouth Neoplasms [MESH:D009062] (2263)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mammary Neoplasms, Animal [MESH:D015674] (3404)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Nervous System Neoplasms [MESH:D009423] (3130)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Limb Deformities, Congenital [MESH:D017880] (1813)   Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Schinzel-Giedion syndrome [MESH:C536632] (16) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Liver Diseases [MESH:D008107] (8167)   Liver Cirrhosis [MESH:D008103] (5542)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Mouth Diseases [MESH:D009059] (4783)   Mouth Neoplasms [MESH:D009062] (2263)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Tooth Diseases [MESH:D014076] (742)   Toothache [MESH:D014098] (46) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Lung Diseases [MESH:D008171] (7249)   Lung Diseases, Interstitial [MESH:D017563] (2966)   Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487) C10. Nervous System Diseases  C10. Nervous System Diseases  Nervous System Diseases [MESH:D009422] (13325)   Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurologic Manifestations [MESH:D009461] (8964)   Neurobehavioral Manifestations [MESH:D019954] (5230)   Intellectual Disability [MESH:D008607] (3054)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eye Diseases, Hereditary [MESH:D015785] (1869)   Leber Congenital Amaurosis [MESH:D057130] (157)   Amaurosis congenita of Leber, type 1 [MESH:C536600] (11)  Retinitis Pigmentosa [MESH:D012174] (414)   Retinal cone dystrophy 2 [MESH:C538363] (11)  Cone-Rod Dystrophy 5 [MESH:C563415] (19)  Retinitis Pigmentosa 13 [MESH:C564008] (30)  Retinal Diseases [MESH:D012164] (3747)   Leber Congenital Amaurosis [MESH:D057130] (157)   Amaurosis congenita of Leber, type 1 [MESH:C536600] (11)  Retinal Degeneration [MESH:D012162] (2386)   Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)   Retinal cone dystrophy 2 [MESH:C538363] (11)  Cone-Rod Dystrophy 5 [MESH:C563415] (19)  Retinitis Pigmentosa 13 [MESH:C564008] (30) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Urogenital Neoplasms [MESH:D014565] (5792)   Urologic Neoplasms [MESH:D014571] (5315)   Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 [MESH:C564400] (37)  Heart Diseases [MESH:D006331] (8614)   Cardiomegaly [MESH:D006332] (4081)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 [MESH:C564400] (37)  Heart Arrest [MESH:D006323] (1926)   Death, Sudden, Cardiac [MESH:D016757] (168)  Heart Defects, Congenital [MESH:D006330] (2443)   Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 [MESH:C564400] (37)  Myocardial Ischemia [MESH:D017202] (5787)   Myocardial Infarction [MESH:D009203] (4122)  Vascular Diseases [MESH:D014652] (8691)   Arteritis [MESH:D001167] (1084)  Hypertension [MESH:D006973] (5655)  Peripheral Vascular Diseases [MESH:D016491] (1412)  Myocardial Ischemia [MESH:D017202] (5791)   Myocardial Infarction [MESH:D009203] (4151)  Vasculitis [MESH:D014657] (2604)   Arteritis [MESH:D001167] (1084) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative [MESH:D054438] (18)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Multiple [MESH:D000015] (3192)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Arrhythmogenic Right Ventricular Dysplasia [MESH:D019571] (241)   Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 [MESH:C564400] (37)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Limb Deformities, Congenital [MESH:D017880] (1813)   Hand Deformities, Congenital [MESH:D006228] (587)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Skin Abnormalities [MESH:D012868] (1723)   Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis bullosa, lethal acantholytic [MESH:C535493] (37)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Eye Diseases, Hereditary [MESH:D015785] (1867)   Retinitis Pigmentosa [MESH:D012174] (442)   Retinal cone dystrophy 2 [MESH:C538363] (11)  Cone-Rod Dystrophy 5 [MESH:C563415] (19)  Retinitis Pigmentosa 13 [MESH:C564008] (30)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Skin Diseases, Genetic [MESH:D012873] (3456)   Skin Fragility-Woolly Hair Syndrome [MESH:C564359] (37)  Epidermolysis Bullosa [MESH:D004820] (259)   Epidermolysis bullosa, lethal acantholytic [MESH:C535493] (37)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Keratosis Palmoplantaris Striata II [MESH:C565102] (37) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Skin Diseases [MESH:D012871] (8774)   Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Drug Eruptions [MESH:D003875] (2697)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hair Diseases [MESH:D006201] (1891)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Skin Fragility-Woolly Hair Syndrome [MESH:C564359] (37)  Keratosis [MESH:D007642] (1941)   Keratoderma, Palmoplantar [MESH:D007645] (287)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Keratosis Palmoplantaris Striata II [MESH:C565102] (37)  Skin Abnormalities [MESH:D012868] (1709)   Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis bullosa, lethal acantholytic [MESH:C535493] (37)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Skin Fragility-Woolly Hair Syndrome [MESH:C564359] (37)  Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis bullosa, lethal acantholytic [MESH:C535493] (37)  Keratoderma, Palmoplantar [MESH:D007645] (287)   Cardiomyopathy dilated with Woolly hair and keratoderma [MESH:C535581] (41)  Keratosis Palmoplantaris Striata II [MESH:C565102] (37)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Epidermolysis Bullosa [MESH:D004820] (260)   Epidermolysis bullosa, lethal acantholytic [MESH:C535493] (37) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Steroid Metabolism, Inborn Errors [MESH:D043202] (962)   Mineralocorticoid Excess Syndrome, Apparent [MESH:D043204] (121)   Apparent mineralocorticoid excess [MESH:C537422] (120)  Nutrition Disorders [MESH:D009748] (4945)   Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Gonadal Disorders [MESH:D006058] (5088)   Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Nails, Malformed [MESH:D009264] (184)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Prolapse [MESH:D011391] (60)   Pelvic Organ Prolapse [MESH:D056887] (59)  Pathologic Processes [MESH:D010335] (9863)   Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)   Death, Sudden, Cardiac [MESH:D016757] (168)  Disease Attributes [MESH:D020969] (3654)   Recurrence [MESH:D012008] (830)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Signs and Symptoms [MESH:D012816] (10659)   Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Neurobehavioral Manifestations [MESH:D019954] (4706)   Intellectual Disability [MESH:D008607] (1476)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Pain [MESH:D010146] (4511)   Facial Pain [MESH:D005157] (56)   Toothache [MESH:D014098] (46) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)  Z. Exceptions (1530)   Not Fully Specified [NFS] (1530) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Psychoses, Substance-Induced [MESH:D011605] (2052) D04. Polycyclic Compounds  D04. Polycyclic Compounds  Polycyclic Compounds [MESH:D011083] (22048)   Steroids [MESH:D013256] (6272)   Pregnanes [MESH:D011278] (1604)   Pregnenes [MESH:D011283] (586)   Pregnenediones [MESH:D011282] (416) F. Psychiatry and Psychology  F. Psychiatry and Psychology  Behavior and Behavior Mechanisms [MESH:D001520] (1594)   Neurobehavioral Manifestations [MESH:D019954] (1206)   Intellectual Disability [MESH:D008607] (1109)   Schinzel-Giedion syndrome [MESH:C536632] (16)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Schinzel-Giedion syndrome [MESH:C536632] (16)