Item 29 of 56 (back to results) previous next   Ceramides D002518               MeSH Unique Identifier: D002518 Scope Notes: Members of the class of neutral glycosphingolipids. They are the basic units of SPHINGOLIPIDS. They are sphingoids attached via their amino groups to a long chain fatty acyl group. They abnormally accumulate in FABRY DISEASE. Chemical – Gene Interaction Note 1: ABCB1 protein inhibits the reaction [Cadmium results in increased abundance of Ceramides] Note 2: ASAH1 gene mutant form results in increased abundance of Ceramides Click here for more information

Current search: C10. Nervous System Diseases: Nervous System Diseases [MESH:D009422] > Central Nervous System Diseases [MESH:D002493] > Brain Diseases [MESH:D001927] > Leukoencephalopathies [MESH:D056784] > Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] > Leukodystrophy, Metachromatic [MESH:D007966] > Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 [HGNC:NFKB1] (254)  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily B [HGNC:ABCB] (452)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  CD molecules [HGNC:CD] (1459)   ATP-binding cassette, sub-family B (MDR/TAP), member 01 [HGNC:ABCB1] (355)  Mitogen-activated protein kinase cascade [HGNC:MAP#K] (854)   Mitogen-activated protein kinase kinase kinases [HGNC:MAP3K] (102)   mitogen-activated protein kinase kinase kinase 5 [HGNC:MAP3K5] (52)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   protein phosphatase 1, regulatory (inhibitor) subunit 01B [HGNC:PPP1R1B] (11)  Serine (or cysteine) peptidase inhibitors [HGNC:SERPIN] (252)   serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 [HGNC:SERPINE1] (138)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor [HGNC:TNF] (795) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   abundance (136)  binding (2423)  cotreatment (1499)  phosphorylation (55)  reaction (624)  secretion (64)  Decreases (5154)   activity (2549)  phosphorylation (590)  reaction (3393)  response to substance (713)  secretion (346)  Increases (5571)   abundance (630)  activity (2865)  phosphorylation (1060)  reaction (1574)  secretion (901) A. Anatomy  A. Anatomy  Cells [MESH:D002477] (1885)   Cellular Structures [MESH:D022082] (1562)   Chromosomes [MESH:D002875] (1300)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Bacteremia [MESH:D016470] (208)  Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Chlamydiaceae Infections [MESH:D002694] (1699)   Chlamydia Infections [MESH:D002690] (1696)  Enterobacteriaceae Infections [MESH:D004756] (669)   Salmonella Infections [MESH:D012480] (620)   Salmonella Infections, Animal [MESH:D012481] (604)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Listeriosis [MESH:D008088] (1622)  Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Leprosy [MESH:D007918] (261)  Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Infection [MESH:D007239] (4109)   Arthritis, Infectious [MESH:D001170] (1702)  Intraabdominal Infections [MESH:D059413] (958)   Appendicitis [MESH:D001064] (774)  Peritonitis [MESH:D010538] (800)  Sepsis [MESH:D018805] (3556)   Bacteremia [MESH:D016470] (1369)  Shock, Septic [MESH:D012772] (1830)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Hepadnaviridae Infections [MESH:D018347] (977)   Hepatitis B [MESH:D006509] (976)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  RNA Virus Infections [MESH:D012327] (4215)   Flaviviridae Infections [MESH:D018178] (1656)   Hepatitis C [MESH:D006526] (1627)  Mononegavirales Infections [MESH:D018701] (900)   Paramyxoviridae Infections [MESH:D018184] (889)   Pneumovirus Infections [MESH:D018186] (853)   Respiratory Syncytial Virus Infections [MESH:D018357] (852)  Picornaviridae Infections [MESH:D010850] (1672)   Cardiovirus Infections [MESH:D018188] (1548)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Slow Virus Diseases [MESH:D012897] (782)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Helminthiasis [MESH:D006373] (1644)   Nematode Infections [MESH:D009349] (870)   Adenophorea Infections [MESH:D017188] (808)   Enoplida Infections [MESH:D017189] (807)   Trichuriasis [MESH:D014257] (805)  Protozoan Infections [MESH:D011528] (3014)   Malaria [MESH:D008288] (2175)  Amebiasis [MESH:D000562] (1711)   Entamoebiasis [MESH:D004749] (1689)  Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)  Hamartoma [MESH:D006222] (1484)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Aggressive [MESH:D018222] (1562)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Carcinoma, Small Cell [MESH:D018288] (1317)  Carcinoma, Squamous Cell [MESH:D002294] (4294)  Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Cholangiocarcinoma [MESH:D018281] (2398)  Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Neoplasms, Basal Cell [MESH:D018295] (1707)   Carcinoma, Basal Cell [MESH:D002280] (1628)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Carcinoma, Squamous Cell [MESH:D002294] (4294)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Retinoblastoma [MESH:D012175] (319)  Glioma [MESH:D005910] (4261)   Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Skin Neoplasms [MESH:D012878] (2992)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Digestive System Neoplasms [MESH:D004067] (7487)   Pancreatic Neoplasms [MESH:D010190] (3820)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Pituitary Neoplasms [MESH:D010911] (981)  Thyroid Neoplasms [MESH:D013964] (2040)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Eye Neoplasms [MESH:D005134] (400)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Head and Neck Neoplasms [MESH:D006258] (4612)   Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1557)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  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)   Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Neoplasms, Multiple Primary [MESH:D009378] (961)   Tuberous Sclerosis [MESH:D014402] (635)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Li-Fraumeni Syndrome [MESH:D016864] (859)  Tuberous Sclerosis [MESH:D014402] (635) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Endocrine [MESH:D001849] (747)   Acromegaly [MESH:D000172] (466)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)   Osteoporosis, Postmenopausal [MESH:D015663] (2351)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)  Spinal Diseases [MESH:D013122] (2485)   Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Infectious [MESH:D001170] (1702)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Muscular Diseases [MESH:D009135] (4071)   Mitochondrial Myopathies [MESH:D017240] (2176)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Rheumatic Diseases [MESH:D012216] (4032)   Arthritis, Rheumatoid [MESH:D001172] (3603) C06. Digestive System Diseases  C06. Digestive System Diseases  Digestive System Diseases [MESH:D004066] (9461)   Biliary Tract Diseases [MESH:D001660] (3845)   Bile Duct Diseases [MESH:D001649] (3512)   Cholestasis [MESH:D002779] (3419)   Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Pancreatic Neoplasms [MESH:D010190] (3820)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Esophageal Neoplasms [MESH:D004938] (3737)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Gastroenteritis [MESH:D005759] (4066)   Appendicitis [MESH:D001064] (774)  Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Adenocarcinoma Of Esophagus [MESH:C562730] (1530)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Appendicitis [MESH:D001064] (774)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Inflammatory Bowel Disease 13 [MESH:C567384] (435)  Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatomegaly [MESH:D006529] (1169)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Fatty Liver [MESH:D005234] (3584)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Hepatic Encephalopathy [MESH:D006501] (1795)  Liver Failure, Acute [MESH:D017114] (2404)  Hepatitis [MESH:D006505] (3883)   Hepatitis, Alcoholic [MESH:D006519] (1613)  Hepatitis, Chronic [MESH:D006521] (2071)   Hepatitis, Autoimmune [MESH:D019693] (1982)  Hepatitis, Viral, Human [MESH:D006525] (1766)   Hepatitis B [MESH:D006509] (976)  Hepatitis C [MESH:D006526] (1627)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Biliary [MESH:D008105] (1274)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Diseases [MESH:D010182] (4453)   Pancreatic Neoplasms [MESH:D010190] (3820)  Peritoneal Diseases [MESH:D010532] (1119)   Peritonitis [MESH:D010538] (800) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Pharyngeal Diseases [MESH:D010608] (1562)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Z. Exceptions (1984)   Not Fully Specified [NFS] (1984)  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Bronchitis [MESH:D001991] (993)   Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Diseases [MESH:D008171] (7249)   Pneumonia [MESH:D011014] (3482)  Pulmonary Edema [MESH:D011654] (2109)  Pulmonary Embolism [MESH:D011655] (1118)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)  Bronchitis [MESH:D001991] (993)   Bronchiolitis [MESH:D001988] (617)   Bronchiolitis Obliterans [MESH:D001989] (611)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Pneumoconiosis [MESH:D011009] (2789)   Anthracosis [MESH:D055008] (1805)  Berylliosis [MESH:D001607] (2005)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Pleural Diseases [MESH:D010995] (2240)   Pleurisy [MESH:D010998] (2070)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Pleurisy [MESH:D010998] (2070)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Legionellosis [MESH:D007876] (612)   Legionnaires' Disease [MESH:D007877] (611)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Bronchial Neoplasms [MESH:D001984] (3608)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380) C09. Otorhinolaryngologic Diseases  C09. Otorhinolaryngologic Diseases  Otorhinolaryngologic Diseases [MESH:D010038] (3827)   Ear Diseases [MESH:D004427] (2522)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Otorhinolaryngologic Neoplasms [MESH:D010039] (1561)   Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Diseases [MESH:D010608] (1605)   Nasopharyngeal Diseases [MESH:D009302] (1508)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198)  Pharyngeal Neoplasms [MESH:D010610] (1520)   Nasopharyngeal Neoplasms [MESH:D009303] (1500)   Nasopharyngeal carcinoma [MESH:C538339] (1198) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Autonomic Nervous System Diseases [MESH:D001342] (882)   Primary Dysautonomias [MESH:D054969] (775)   Orthostatic Intolerance [MESH:D054971] (720)   Hypotension, Orthostatic [MESH:D007024] (679)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Embolism and Thrombosis [MESH:D002542] (490)   Intracranial Thrombosis [MESH:D020767] (481)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Encephalitis [MESH:D004660] (226)   Meningoencephalitis [MESH:D008590] (179)  Epilepsy [MESH:D004827] (6274)   Status Epilepticus [MESH:D013226] (4014)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)  Hypothalamic Diseases [MESH:D007027] (1833)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Pituitary Diseases [MESH:D010900] (1808)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1250)   Acromegaly [MESH:D000172] (466)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Central Nervous System Infections [MESH:D002494] (1823)   Meningoencephalitis [MESH:D008590] (207)  Encephalitis [MESH:D004660] (351)   Meningoencephalitis [MESH:D008590] (179)  Meningitis [MESH:D008581] (1506)   Meningoencephalitis [MESH:D008590] (179)  Meningitis [MESH:D008581] (352)   Meningoencephalitis [MESH:D008590] (179)  Movement Disorders [MESH:D009069] (4823)   Dyskinesias [MESH:D020820] (1827)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Compression [MESH:D013117] (1800)  Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Cerebral Ventricle Neoplasms [MESH:D002551] (772)   Choroid Plexus Neoplasms [MESH:D016545] (771)   Papilloma, Choroid Plexus [MESH:D020288] (769)  Supratentorial Neoplasms [MESH:D015173] (930)   Hypothalamic Neoplasms [MESH:D007029] (922)   Pituitary Neoplasms [MESH:D010911] (914)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Tuberous Sclerosis [MESH:D014402] (635)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Tuberous Sclerosis [MESH:D014402] (635)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Paralysis [MESH:D010243] (2043)  Paresis [MESH:D010291] (419)  Dyskinesias [MESH:D020820] (3365)   Catalepsy [MESH:D002375] (1429)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)   Aphasia [MESH:D001037] (219)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3875)   Neuralgia [MESH:D009437] (2074)  Back Pain [MESH:D001416] (287)   Low Back Pain [MESH:D017116] (244)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Diseases [MESH:D009135] (3538)   Mitochondrial Myopathies [MESH:D017240] (2176)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neuralgia [MESH:D009437] (2078)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)  Eyelid Diseases [MESH:D005141] (882)  Eye Neoplasms [MESH:D005134] (413)   Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Retinal Diseases [MESH:D012164] (3747)   Retinal Detachment [MESH:D012163] (1639)  Retinal Neoplasms [MESH:D019572] (320)   Retinoblastoma [MESH:D012175] (319)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Testicular Diseases [MESH:D013733] (451)  Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Z. Exceptions (1116)   Not Fully Specified [NFS] (1116)  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)  Ovarian Neoplasms [MESH:D010051] (3281)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Sexually Transmitted Diseases [MESH:D012749] (1712)   Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711)   Chlamydia Infections [MESH:D002690] (1693)  Vulvar Diseases [MESH:D014845] (873)   Vulvar Lichen Sclerosus [MESH:D007724] (825)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Diabetic Nephropathies [MESH:D003928] (2301)  Hyperoxaluria [MESH:D006959] (1498)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephritis, Interstitial [MESH:D009395] (1927)   Balkan Nephropathy [MESH:D001449] (772)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)   Kidney Tubular Necrosis, Acute [MESH:D007683] (974)  Renal Insufficiency, Chronic [MESH:D051436] (2931)   Kidney Failure, Chronic [MESH:D007676] (2930)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Placenta Diseases [MESH:D010922] (1781)  Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)  Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Heart Diseases [MESH:D006331] (8614)   Cardiac Tamponade [MESH:D002305] (175)  Heart Arrest [MESH:D006323] (1926)  Heart Failure [MESH:D006333] (4058)  Pericardial Effusion [MESH:D010490] (1015)  Ventricular Dysfunction [MESH:D018754] (2348)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Tachycardia [MESH:D013610] (3339)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocarditis [MESH:D009205] (1708)  Heart Defects, Congenital [MESH:D006330] (2443)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Thrombosis [MESH:D003328] (255)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4122)   Myocardial Stunning [MESH:D017682] (1816)  Shock, Cardiogenic [MESH:D012770] (269)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Hypertension [MESH:D006973] (5655)  Vascular System Injuries [MESH:D057772] (2086)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Vasospasm, Intracranial [MESH:D020301] (324)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212)  Stroke [MESH:D020521] (3702)   Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Embolism and Thrombosis [MESH:D016769] (3374)   Embolism [MESH:D004617] (1137)   Pulmonary Embolism [MESH:D011655] (1118)  Embolism, Fat [MESH:D004620] (261)   Embolism, Cholesterol [MESH:D017700] (255)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Thrombosis [MESH:D013927] (3101)   Coronary Thrombosis [MESH:D003328] (255)  Venous Thrombosis [MESH:D020246] (1141)  Thromboembolism [MESH:D013923] (732)   Venous Thromboembolism [MESH:D054556] (400)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)  Hypotension [MESH:D007022] (4045)   Hypotension, Orthostatic [MESH:D007024] (679)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Stunning [MESH:D017682] (1816)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Coronary Disease [MESH:D003327] (3439)   Coronary Thrombosis [MESH:D003328] (255)  Coronary Stenosis [MESH:D023921] (1806)   Coronary Restenosis [MESH:D023903] (1683)  Myocardial Infarction [MESH:D009203] (4151)   Myocardial Stunning [MESH:D017682] (1816)  Shock, Cardiogenic [MESH:D012770] (269)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Refractory [MESH:D000753] (1567)  Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Anemia, Hemolytic [MESH:D000743] (3083)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)  Bone Marrow Diseases [MESH:D001855] (2944)   Anemia, Aplastic [MESH:D000741] (1925)   Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Refractory [MESH:D000753] (1567)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Hemorrhagic Disorders [MESH:D006474] (3359)   Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Leukocyte Disorders [MESH:D007960] (2662)   Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)  Lymphatic Diseases [MESH:D008206] (5167)   Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) 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)   Down Syndrome [MESH:D004314] (1287)  LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Nervous System Malformations [MESH:D009421] (3354)   Neural Tube Defects [MESH:D009436] (2143)  Malformations of Cortical Development [MESH:D054220] (1406)   Tuberous Sclerosis [MESH:D014402] (635)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Anemia, Sickle Cell [MESH:D000755] (1722)  Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)   Fanconi Anemia [MESH:D005199] (1604)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Tuberous Sclerosis [MESH:D014402] (635)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Fragile X Syndrome [MESH:D005600] (353)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Li-Fraumeni Syndrome [MESH:D016864] (859)  Tuberous Sclerosis [MESH:D014402] (635)  Skin Diseases, Genetic [MESH:D012873] (3456)   Dermatitis, Atopic [MESH:D003876] (2052) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Scleroderma, Localized [MESH:D012594] (1597)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 5 [MESH:C548083] (169)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Keratosis [MESH:D007642] (1941)  Scleroderma, Localized [MESH:D012594] (1597)  Skin Neoplasms [MESH:D012878] (2991)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)   LEOPARD syndrome, 2 [MESH:C537117] (169)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Dermatitis, Atopic [MESH:D003876] (2052)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)   Leishmaniasis, Mucocutaneous [MESH:D007897] (606)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Brain Diseases, Metabolic [MESH:D001928] (3350)   Hepatic Encephalopathy [MESH:D006501] (1795)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Hypercalcemia [MESH:D006934] (1999)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Fanconi Anemia [MESH:D005199] (1604)  Li-Fraumeni Syndrome [MESH:D016864] (859)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Hypoglycemia [MESH:D007003] (2420)  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)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)   Hemochromatosis [MESH:D006432] (1694)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Hyperlipoproteinemias [MESH:D006951] (903)  Hypertriglyceridemia [MESH:D015228] (808)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Malabsorption Syndromes [MESH:D008286] (1869)   Hyperhomocysteinemia [MESH:D020138] (1716)  Metabolic Syndrome X [MESH:D024821] (2151)   Abdominal obesity metabolic syndrome [MESH:C535554] (359)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Hyperhomocysteinemia [MESH:D020138] (1724)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Adrenoleukodystrophy [MESH:D000326] (1348)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipidemia, Familial Combined [MESH:D006950] (372)  Lipidoses [MESH:D008064] (1655)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Farber Lipogranulomatosis [MESH:D055577] (62)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type A [MESH:D052536] (44)  Niemann-Pick Disease, Type B [MESH:D052537] (44)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Hemochromatosis [MESH:D006432] (1694)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Mitochondrial Diseases [MESH:D028361] (2561)   Mitochondrial Myopathies [MESH:D017240] (2176)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hypercalcemia [MESH:D006934] (1999)  Hyponatremia [MESH:D007010] (789)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Hyperhomocysteinemia [MESH:D020138] (1716)  Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)  Wasting Syndrome [MESH:D019282] (1959)   HIV Wasting Syndrome [MESH:D019247] (1956) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Cortex Diseases [MESH:D000303] (969)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  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)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Neuropathies [MESH:D003929] (2443)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)  Pituitary Neoplasms [MESH:D010911] (981)  Thyroid Neoplasms [MESH:D013964] (2040)  Adrenal Gland Neoplasms [MESH:D000310] (917)   Adrenal Cortex Neoplasms [MESH:D000306] (823)   Adrenocortical Carcinoma [MESH:D018268] (821)   Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769)  Gonadal Disorders [MESH:D006058] (5088)   Puberty, Precocious [MESH:D011629] (1147)  Testicular Diseases [MESH:D013733] (777)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Cysts [MESH:D010048] (2534)  Ovarian Neoplasms [MESH:D010051] (3281)  Pituitary Diseases [MESH:D010900] (1829)   Pituitary Neoplasms [MESH:D010911] (981)  Hyperpituitarism [MESH:D006964] (1259)   Acromegaly [MESH:D000172] (466)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Thyroid Neoplasms [MESH:D013964] (2040) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Graft vs Host Disease [MESH:D006086] (674)  Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Hepatitis, Autoimmune [MESH:D019693] (1982)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)  Hypersensitivity, Delayed [MESH:D006968] (3408)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Dermatitis, Atopic [MESH:D003876] (2052)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)   Acquired Immunodeficiency Syndrome [MESH:D000163] (743)  HIV Wasting Syndrome [MESH:D019247] (1956)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Leukemia, Lymphoid [MESH:D007945] (3047)   Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)  Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Mantle-Cell [MESH:D020522] (561)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735)  Salmonella Infections, Animal [MESH:D012481] (604) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Amyloid [MESH:D058225] (334)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Hepatomegaly [MESH:D006529] (1169)  Pathologic Processes [MESH:D010335] (9863)   Emphysema [MESH:D004646] (1096)  Fibrosis [MESH:D005355] (3133)  Gliosis [MESH:D005911] (1419)  Hyperbilirubinemia [MESH:D006932] (1860)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Tachycardia [MESH:D013610] (3339)  Chromosome Aberrations [MESH:D002869] (2352)   Translocation, Genetic [MESH:D014178] (557)  Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Growth Disorders [MESH:D006130] (2438)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Hemorrhage [MESH:D006470] (4451)   Shock, Hemorrhagic [MESH:D012771] (2042)  Hematoma [MESH:D006406] (281)   Hematoma, Epidural, Spinal [MESH:D046748] (167)  Hematoma, Subdural [MESH:D006408] (215)  Intracranial Hemorrhages [MESH:D020300] (3241)   Hematoma, Subdural [MESH:D006408] (212)  Cerebral Hemorrhage [MESH:D002543] (2872)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Bacteremia [MESH:D016470] (1369)  Shock, Septic [MESH:D012772] (1830)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Postoperative Complications [MESH:D011183] (5311)   Pain, Postoperative [MESH:D010149] (529)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Multiple Organ Failure [MESH:D009102] (1836)  Shock, Cardiogenic [MESH:D012770] (269)  Shock, Hemorrhagic [MESH:D012771] (2042)  Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Chills [MESH:D023341] (644)  Edema [MESH:D004487] (3726)  Flushing [MESH:D005483] (506)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Neurologic Manifestations [MESH:D009461] (8702)   Paralysis [MESH:D010243] (2298)  Paresis [MESH:D010291] (419)  Dyskinesias [MESH:D020820] (3285)   Catalepsy [MESH:D002375] (1429)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Intellectual Disability [MESH:D008607] (1476)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)   Aphasia [MESH:D001037] (219)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Pain [MESH:D010146] (3869)   Neuralgia [MESH:D009437] (2074)  Back Pain [MESH:D001416] (285)   Low Back Pain [MESH:D017116] (244)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sensorineural [MESH:D006319] (1227)   Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Neuralgia [MESH:D009437] (2074)  Pain, Postoperative [MESH:D010149] (529)  Back Pain [MESH:D001416] (285)   Low Back Pain [MESH:D017116] (244)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Stable [MESH:D060050] (1702)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Nausea [MESH:D009325] (2300)  Vomiting [MESH:D014839] (1354)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)   Albuminuria [MESH:D000419] (2394) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Berylliosis [MESH:D001607] (2005) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug Hypersensitivity [MESH:D004342] (4001)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Neurotoxicity Syndromes [MESH:D020258] (3323)  Substance-Related Disorders [MESH:D019966] (6308)   Amphetamine-Related Disorders [MESH:D019969] (2858)  Cocaine-Related Disorders [MESH:D019970] (3054)  Marijuana Abuse [MESH:D002189] (1132)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Fatty Liver, Alcoholic [MESH:D005235] (657)  Hepatitis, Alcoholic [MESH:D006519] (1613)  Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Burns [MESH:D002056] (2565)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (217)   Hematoma, Subdural [MESH:D006408] (212)  Radiation Injuries [MESH:D011832] (2718)   Radiation Injuries, Experimental [MESH:D011833] (2662)  Spinal Cord Injuries [MESH:D013119] (2688)   Spinal Cord Compression [MESH:D013117] (1800)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431)  Intracranial Hemorrhage, Traumatic [MESH:D020198] (221)   Hematoma, Subdural [MESH:D006408] (212) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Amides [MESH:D000577] (5297)   Ceramides [MESH:D002518] (234) D09. Carbohydrates  D09. Carbohydrates  Carbohydrates [MESH:D002241] (15391)   Glycoconjugates [MESH:D006001] (1937)   Glycolipids [MESH:D006017] (760)   Glycosphingolipids [MESH:D006028] (510)   Neutral Glycosphingolipids [MESH:D020383] (267)   Ceramides [MESH:D002518] (234) D10. Lipids  D10. Lipids  Lipids [MESH:D008055] (8597)   Glycolipids [MESH:D006017] (808)   Glycosphingolipids [MESH:D006028] (510)   Neutral Glycosphingolipids [MESH:D020383] (267)   Ceramides [MESH:D002518] (234)  Membrane Lipids [MESH:D008563] (2387)   Sphingolipids [MESH:D013107] (529)   Glycosphingolipids [MESH:D006028] (510)   Neutral Glycosphingolipids [MESH:D020383] (267)   Ceramides [MESH:D002518] (234) G. Phenomena and Processes  G. Phenomena and Processes  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 16-18 [MESH:D002902] (799)   Chromosomes, Human, Pair 17 [MESH:D002886] (779)   Chromosome 17 deletion [MESH:C538045] (769)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   Allelic Imbalance [MESH:D022981] (1120)   Loss of Heterozygosity [MESH:D019656] (1119)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   Chromosome 17 deletion [MESH:C538045] (769)