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 clopidogrel
C055162
 
  
  
  

MeSH Unique Identifier: C055162
Chemical – Gene Interaction

Note 1: ABCB1 gene affects the reaction [CYP2C19 gene affects the susceptibility to clopidogrel]

Note 2: ABCB1 gene affects the susceptibility to clopidogrel

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1. Human Genes 
1. Human Genes
 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)
 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) [HGNC:ITGA2] (42)
 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [HGNC:ITGB3] (49)
 Chemokine ligands [HGNC:CCL] (472) 
 chemokine (C-C motif) ligand 04 [HGNC:CCL4] (96)
 chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141)
 Cytochrome P450s [HGNC:CYP] (1673) 
 cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466)
 cytochrome P450, family 02, subfamily B, polypeptide 06 [HGNC:CYP2B6] (216)
 cytochrome P450, family 02, subfamily C, polypeptide 08 [HGNC:CYP2C8] (106)
 cytochrome P450, family 02, subfamily C, polypeptide 09 [HGNC:CYP2C9] (220)
 cytochrome P450, family 02, subfamily C, polypeptide 19 [HGNC:CYP2C19] (172)
 cytochrome P450, family 02, subfamily D, polypeptide 06 [HGNC:CYP2D6] (200)
 cytochrome P450, family 03, subfamily A, polypeptide 04 [HGNC:CYP3A4] (612)
 cytochrome P450, family 03, subfamily A, polypeptide 05 [HGNC:CYP3A5] (134)
 Endogenous Ligands [HGNC:ENDOLIG] (1191) 
 chemokine (C-C motif) ligand 04 [HGNC:CCL4] (96)
 chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141)
 Integrins [HGNC:ITG] (284) 
 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) [HGNC:ITGA2] (42)
 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61) [HGNC:ITGB3] (49)
 Interferons and interferon receptors [HGNC:IFN] (684) 
 interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)
 Interleukins and interleukin receptors [HGNC:IL] (1294) 
 interleukin 06 (interferon, beta 2) [HGNC:IL6] (511)
 Paraoxonases [HGNC:PON] (134) 
 paraoxonase 1 [HGNC:PON1] (115)
 Protease activated receptors [HGNC:F2R] (81) 
 coagulation factor II (thrombin) receptor [HGNC:F2R] (49)
 Purinergic receptors [HGNC:P2R] (49) 
 Purinergic receptors, P2Y [HGNC:P2RY] (25) 
 purinergic receptor P2Y, G-protein coupled, 12 [HGNC:P2RY12] (6)
2. Interaction: Human Genes and Chemicals 
2. Interaction: Human Genes and Chemicals
 Affects (3990) 
 abundance (136)
 binding (2423)
 cotreatment (1499)
 phosphorylation (55)
 reaction (624)
 response to substance (623)
 Decreases (5154) 
 activity (2549)
 expression (2187)
 metabolic processing (88)
 reaction (3393)
 response to substance (713)
 secretion (346)
 uptake (71)
 Increases (5571) 
 activity (2865)
 cleavage (666)
 degradation (347)
 expression (3238)
 metabolic processing (740)
 oxidation (295)
 reaction (1574)
 response to substance (641)
 secretion (901)
A. Anatomy 
A. Anatomy
 Musculoskeletal System [MESH:D009141] (1255) 
 Skeleton [MESH:D012863] (1177) 
 Bone and Bones [MESH:D001842] (1112) 
 Skull [MESH:D012886] (610) 
 Facial Bones [MESH:D005147] (539) 
 Jaw [MESH:D007568] (524) 
 Mandible [MESH:D008334] (511) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
 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)
 Chromosomes, Human, 21-22 and Y [MESH:D002904] (294) 
 Chromosomes, Human, Pair 21 [MESH:D002891] (58) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Stomatognathic System [MESH:D013284] (673) 
 Jaw [MESH:D007568] (528) 
 Mandible [MESH:D008334] (511) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
C01. Bacterial Infections and Mycoses 
C01. Bacterial Infections and Mycoses
 Bacterial Infections [MESH:D001424] (3716) 
 Gram-Negative Bacterial Infections [MESH:D016905] (3085) 
 Chlamydiaceae Infections [MESH:D002694] (1699) 
 Chlamydia Infections [MESH:D002690] (1696)
 Gram-Positive Bacterial Infections [MESH:D016908] (2434) 
 Listeriosis [MESH:D008088] (1622)
 Actinomycetales Infections [MESH:D000193] (1466) 
 Mycobacterium Infections [MESH:D009164] (1446) 
 Paratuberculosis [MESH:D010283] (427)
 Tuberculosis [MESH:D014376] (992) 
 Tuberculosis, Bovine [MESH:D014380] (380)
 Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711) 
 Chlamydia Infections [MESH:D002690] (1693)
 Infection [MESH:D007239] (4109) 
 Arthritis, Infectious [MESH:D001170] (1702)
 Sepsis [MESH:D018805] (3556) 
 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) 
 Central Nervous System Viral Diseases [MESH:D020805] (1416) 
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 DNA Virus Infections [MESH:D004266] (2474) 
 Herpesviridae Infections [MESH:D006566] (1944) 
 Sarcoma, Kaposi [MESH:D012514] (1578)
 Hepatitis, Viral, Human [MESH:D006525] (1766) 
 Hepatitis C [MESH:D006526] (1627)
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 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) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Sexually Transmitted Diseases [MESH:D012749] (3305) 
 Sexually Transmitted Diseases, Viral [MESH:D015229] (3304) 
 HIV Infections [MESH:D015658] (3296) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
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, Cutaneous [MESH:D016773] (2359)
 Leishmaniasis, Visceral [MESH:D007898] (2149)
 Skin Diseases, Parasitic [MESH:D012876] (2541) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359)
C04. Neoplasms 
C04. Neoplasms
 Neoplasms [MESH:D009369] (10293) 
 Precancerous Conditions [MESH:D011230] (2858)
 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)
 Lymphoma [MESH:D008223] (3686) 
 Lymphoma, Non-Hodgkin [MESH:D008228] (3337) 
 Lymphoma, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Neoplasms, Complex and Mixed [MESH:D018193] (1121) 
 Carcinosarcoma [MESH:D002296] (581)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 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) 
 Carcinosarcoma [MESH:D002296] (581)
 Hemangiosarcoma [MESH:D006394] (1836)
 Osteosarcoma [MESH:D012516] (2175)
 Sarcoma, Kaposi [MESH:D012514] (1578)
 Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126) 
 Neuroectodermal Tumors [MESH:D017599] (5066) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Gliosarcoma [MESH:D018316] (880)
 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)
 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, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Gliosarcoma [MESH:D018316] (880)
 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)
 Papilloma [MESH:D010212] (2243)
 Neoplasms, Nerve Tissue [MESH:D009380] (5201) 
 Neuroectodermal Tumors [MESH:D017599] (5059) 
 Neoplasms, Neuroepithelial [MESH:D018302] (4487) 
 Glioma [MESH:D005910] (4261) 
 Gliosarcoma [MESH:D018316] (880)
 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, Plasma Cell [MESH:D054219] (2772) 
 Multiple Myeloma [MESH:D009101] (2767)
 Neoplasms, Vascular Tissue [MESH:D009383] (2959) 
 Hemangiosarcoma [MESH:D006394] (1836)
 Sarcoma, Kaposi [MESH:D012514] (1578)
 Nevi and Melanomas [MESH:D018326] (3572) 
 Melanoma [MESH:D008545] (3508)
 Neoplasms by Site [MESH:D009371] (9169) 
 Bone Neoplasms [MESH:D001859] (1334)
 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)
 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)
 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)
 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)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Neoplasms, Experimental [MESH:D009374] (5218) 
 Liver Neoplasms, Experimental [MESH:D008114] (2837)
 Mammary Neoplasms, Experimental [MESH:D008325] (3268)
 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)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
C05. Musculoskeletal Diseases 
C05. Musculoskeletal Diseases
 Musculoskeletal Diseases [MESH:D009140] (8705) 
 Bone Diseases [MESH:D001847] (5801) 
 Bone Neoplasms [MESH:D001859] (1334)
 Bone Diseases, Developmental [MESH:D001848] (3315) 
 Acromicric dysplasia [MESH:C535662] (520)
 Marfan Syndrome [MESH:D008382] (646)
 Acro-Osteolysis [MESH:D030981] (548) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
 Osteochondrodysplasias [MESH:D010009] (2440) 
 Metaphyseal Anadysplasia 2 [MESH:C567771] (452)
 Camurati-Engelmann Syndrome [MESH:D003966] (492)
 Osteosclerosis [MESH:D010026] (356) 
 Osteopetrosis [MESH:D010022] (318)
 Bone Diseases, Metabolic [MESH:D001851] (3492) 
 Osteoporosis [MESH:D010024] (3037) 
 Osteoporosis, Postmenopausal [MESH:D015663] (2351)
 Bone Resorption [MESH:D001862] (2352) 
 Osteolysis [MESH:D010014] (1787) 
 Acro-Osteolysis [MESH:D030981] (548) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
 Spinal Diseases [MESH:D013122] (2485) 
 Intervertebral Disc Degeneration [MESH:D055959] (827) 
 Intervertebral disc disease [MESH:C535531] (514)
 Intervertebral Disc Displacement [MESH:D007405] (520) 
 Intervertebral disc disease [MESH:C535531] (514)
 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, Juvenile [MESH:D001171] (1060)
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
 Spondylarthritis [MESH:D025241] (1912) 
 Spondylarthropathies [MESH:D025242] (1909) 
 Arthritis, Psoriatic [MESH:D015535] (1859)
 Muscular Diseases [MESH:D009135] (4071) 
 Compartment Syndromes [MESH:D003161] (80)
 Mitochondrial Myopathies [MESH:D017240] (2176)
 Muscle Rigidity [MESH:D009127] (617)
 Rhabdomyolysis [MESH:D012206] (465)
 Muscular Disorders, Atrophic [MESH:D020966] (1598) 
 Muscular Dystrophies [MESH:D009136] (1593) 
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 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) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 Acromicric dysplasia [MESH:C535662] (520)
 Metaphyseal Anadysplasia 2 [MESH:C567771] (452)
 Rheumatic Diseases [MESH:D012216] (4032) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Osteoarthritis [MESH:D010003] (1743)
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 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) 
 Esophageal Neoplasms [MESH:D004938] (3737) 
 Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
 Gastroenteritis [MESH:D005759] (4066) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Inflammatory Bowel Diseases [MESH:D015212] (3492) 
 Inflammatory Bowel Disease 13 [MESH:C567384] (435)
 Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43)
 Colitis, Ulcerative [MESH:D003093] (2601)
 Crohn Disease [MESH:D003424] (2585)
 Gastrointestinal Hemorrhage [MESH:D006471] (815) 
 Peptic Ulcer Hemorrhage [MESH:D010438] (553)
 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) 
 Colonic Diseases [MESH:D003108] (5564) 
 Colitis [MESH:D003092] (3199) 
 Colitis, Ulcerative [MESH:D003093] (2601)
 Colorectal Neoplasms [MESH:D015179] (5282) 
 Colonic Neoplasms [MESH:D003110] (4405)
 Duodenal Diseases [MESH:D004378] (1982) 
 Peptic Ulcer [MESH:D010437] (1969) 
 Duodenal Ulcer [MESH:D004381] (1549)
 Inflammatory Bowel Diseases [MESH:D015212] (3492) 
 Inflammatory Bowel Disease 13 [MESH:C567384] (435)
 Inflammatory Bowel Disease 28, Autosomal Recessive [MESH:C567728] (43)
 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)
 Hemorrhoids [MESH:D006484] (166)
 Peptic Ulcer [MESH:D010437] (3172) 
 Duodenal Ulcer [MESH:D004381] (1549)
 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)
 Hepatic Veno-Occlusive Disease [MESH:D006504] (208)
 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) 
 Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)
 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 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) 
 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)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Pancreatic Diseases [MESH:D010182] (4453) 
 Cystic Fibrosis [MESH:D003550] (760)
 Pancreatic Neoplasms [MESH:D010190] (3820)
 Pancreatitis [MESH:D010195] (1924)
 Peritoneal Diseases [MESH:D010532] (1119) 
 Peritoneal Fibrosis [MESH:D056627] (488)
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)
 Periodontal Diseases [MESH:D010510] (1001) 
 Periodontitis [MESH:D010518] (843)
 Gingival Diseases [MESH:D005882] (217) 
 Gingival Overgrowth [MESH:D019214] (192) 
 Gingival Hyperplasia [MESH:D005885] (161)
 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)
 Lung Diseases [MESH:D008171] (7249) 
 Cystic Fibrosis [MESH:D003550] (760)
 Hypertension, Pulmonary [MESH:D006976] (2000)
 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) 
 Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102)
 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) 
 Pulmonary Emphysema [MESH:D011656] (1259)
 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)
 Pulmonary Alveolar Proteinosis [MESH:D011649] (139) 
 Surfactant Metabolism Dysfunction, Pulmonary, 1 [MESH:C566882] (102)
 Nose Diseases [MESH:D009668] (1504) 
 Paranasal Sinus Diseases [MESH:D010254] (476) 
 Sinusitis [MESH:D012852] (469)
 Rhinitis [MESH:D012220] (1134) 
 Rhinitis, Allergic, Perennial [MESH:D012221] (625) 
 Allergic Rhinitis [MESH:C567078] (181)
 Pleural Diseases [MESH:D010995] (2240) 
 Pleurisy [MESH:D010998] (2070)
 Respiration Disorders [MESH:D012120] (2218) 
 Dyspnea [MESH:D004417] (248)
 Apnea [MESH:D001049] (748) 
 Sleep Apnea Syndromes [MESH:D012891] (570) 
 Sleep Apnea, Central [MESH:D020182] (347) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Respiratory Insufficiency [MESH:D012131] (841) 
 Hypoventilation [MESH:D007040] (360) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Respiratory Hypersensitivity [MESH:D012130] (4401) 
 Ige Responsiveness, Atopic [MESH:C564133] (267)
 Asthma [MESH:D001249] (4098)
 Rhinitis, Allergic, Perennial [MESH:D012221] (625) 
 Allergic Rhinitis [MESH:C567078] (181)
 Respiratory Tract Infections [MESH:D012141] (3926) 
 Pleurisy [MESH:D010998] (2070)
 Pneumonia [MESH:D011014] (3482)
 Rhinitis [MESH:D012220] (766)
 Sinusitis [MESH:D012852] (469)
 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) 
 Deafness [MESH:D003638] (623)
 Nose Diseases [MESH:D009668] (1504) 
 Paranasal Sinus Diseases [MESH:D010254] (476) 
 Sinusitis [MESH:D012852] (469)
 Rhinitis [MESH:D012220] (1134) 
 Rhinitis, Allergic, Perennial [MESH:D012221] (625) 
 Allergic Rhinitis [MESH:C567078] (181)
 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) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 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 Edema [MESH:D001929] (1165)
 Brain Injuries [MESH:D001930] (3429)
 Basal Ganglia Diseases [MESH:D001480] (4268) 
 Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Parkinson Disease [MESH:D010300] (3595)
 Brain Diseases, Metabolic [MESH:D001928] (3351) 
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)
 Brain Neoplasms [MESH:D001932] (2764) 
 Cerebral Ventricle Neoplasms [MESH:D002551] (772) 
 Choroid Plexus Neoplasms [MESH:D016545] (771) 
 Papilloma, Choroid Plexus [MESH:D020288] (769)
 Cerebrovascular Disorders [MESH:D002561] (5542) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Vertebrobasilar Insufficiency [MESH:D014715] (9)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Carotid Artery Diseases [MESH:D002340] (1993) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Carotid Stenosis [MESH:D016893] (174)
 Intracranial Arterial Diseases [MESH:D020765] (2463) 
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Embolism and Thrombosis [MESH:D002542] (490) 
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Subarachnoid Hemorrhage [MESH:D013345] (1082)
 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)
 Epilepsy [MESH:D004827] (6274) 
 Seizures [MESH:D012640] (4502)
 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)
 Central Nervous System Infections [MESH:D002494] (1823) 
 Central Nervous System Viral Diseases [MESH:D020805] (1416) 
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Meningitis [MESH:D008581] (1506) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Meningitis, Viral [MESH:D008587] (1308) 
 Meningitis, Aseptic [MESH:D008582] (1305)
 Movement Disorders [MESH:D009069] (4823) 
 Parkinsonian Disorders [MESH:D020734] (4009) 
 Parkinson Disease [MESH:D010300] (3595)
 Spinal Cord Diseases [MESH:D013118] (4376) 
 Spinal Cord Compression [MESH:D013117] (1800)
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)
 Spinal Cord Vascular Diseases [MESH:D020758] (14) 
 Spinal Cord Ischemia [MESH:D020760] (12)
 Demyelinating Diseases [MESH:D003711] (2917) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Nervous System Malformations [MESH:D009421] (3354) 
 Central Nervous System Vascular Malformations [MESH:D020785] (1031) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Neural Tube Defects [MESH:D009436] (2143) 
 Spinal Dysraphism [MESH:D016135] (1025)
 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)
 Neurodegenerative Diseases [MESH:D019636] (6613) 
 Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)
 Parkinson Disease [MESH:D010300] (3595)
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)
 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)
 Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)
 Neurologic Manifestations [MESH:D009461] (8964) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Seizures [MESH:D012640] (4514)
 Dyskinesias [MESH:D020820] (3365) 
 Dystonia [MESH:D004421] (848)
 Tremor [MESH:D014202] (840)
 Neurobehavioral Manifestations [MESH:D019954] (5230) 
 Consciousness Disorders [MESH:D003244] (680) 
 Unconsciousness [MESH:D014474] (660) 
 Coma [MESH:D003128] (524)
 Syncope [MESH:D013575] (128)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (3054) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Perceptual Disorders [MESH:D010468] (343) 
 Hallucinations [MESH:D006212] (251)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscle Hypertonia [MESH:D009122] (775) 
 Muscle Rigidity [MESH:D009127] (617)
 Muscle Hypotonia [MESH:D009123] (258) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Pain [MESH:D010146] (3875) 
 Headache [MESH:D006261] (1416)
 Neuralgia [MESH:D009437] (2074)
 Sensation Disorders [MESH:D012678] (5011) 
 Hearing Disorders [MESH:D006311] (2103) 
 Hearing Loss [MESH:D034381] (2068) 
 Deafness [MESH:D003638] (623)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Hypesthesia [MESH:D006987] (58)
 Taste Disorders [MESH:D013651] (461) 
 Ageusia [MESH:D000370] (20)
 Neuromuscular Diseases [MESH:D009468] (7336) 
 Motor Neuron Disease [MESH:D016472] (3670) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)
 Muscular Diseases [MESH:D009135] (3538) 
 Mitochondrial Myopathies [MESH:D017240] (2176)
 Muscular Disorders, Atrophic [MESH:D020966] (1594) 
 Muscular Dystrophies [MESH:D009136] (1589) 
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 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)
 Sleep Disorders [MESH:D012893] (2050) 
 Dyssomnias [MESH:D020920] (1417) 
 Sleep Disorders, Intrinsic [MESH:D020919] (1270) 
 Sleep Apnea Syndromes [MESH:D012891] (570) 
 Sleep Apnea, Central [MESH:D020182] (347) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Trauma, Nervous System [MESH:D020196] (3997) 
 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) 
 Eye Abnormalities [MESH:D005124] (1233) 
 Aniridia [MESH:D015783] (312) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Eye Diseases, Hereditary [MESH:D015785] (1869) 
 Aniridia [MESH:D015783] (312) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Lacrimal Apparatus Diseases [MESH:D007766] (644) 
 Dry Eye Syndromes [MESH:D015352] (533)
 Retinal Diseases [MESH:D012164] (3747) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Retinal Vein Occlusion [MESH:D012170] (607)
 Uveal Diseases [MESH:D014603] (2428) 
 Iris Diseases [MESH:D007499] (348) 
 Aniridia [MESH:D015783] (312) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 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) 
 Genital Neoplasms, Male [MESH:D005834] (6224) 
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Neoplasms [MESH:D011471] (6135)
 Infertility [MESH:D007246] (2909) 
 Infertility, Male [MESH:D007248] (2851)
 Penile Diseases [MESH:D010409] (1805) 
 Penile Induration [MESH:D010411] (495)
 Penile Neoplasms [MESH:D010412] (890)
 Prostatic Diseases [MESH:D011469] (6204) 
 Prostatic Neoplasms [MESH:D011471] (6135)
 Sexually Transmitted Diseases [MESH:D012749] (1712) 
 Sexually Transmitted Diseases, Bacterial [MESH:D015231] (1711) 
 Chlamydia Infections [MESH:D002690] (1693)
 Urogenital Abnormalities [MESH:D014564] (2065) 
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 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)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 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)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
 Lupus Nephritis [MESH:D008181] (602)
 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)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Renal Aminoacidurias [MESH:D000608] (95) 
 Cystinuria [MESH:D003555] (67) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Ureteral Diseases [MESH:D014515] (1024) 
 Ureteral Obstruction [MESH:D014517] (575)
 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
 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 Neoplasms [MESH:D010051] (3281)
 Primary Ovarian Insufficiency [MESH:D016649] (270)
 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 Abnormalities [MESH:D014564] (2043) 
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 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)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 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)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Nephritis [MESH:D009393] (4236) 
 Glomerulonephritis [MESH:D005921] (3758) 
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
 Lupus Nephritis [MESH:D008181] (602)
 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)
 Renal Insufficiency, Chronic [MESH:D051436] (2931) 
 Kidney Failure, Chronic [MESH:D007676] (2930)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058) 
 Renal Aminoacidurias [MESH:D000608] (95) 
 Cystinuria [MESH:D003555] (67) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Uremia [MESH:D014511] (2898) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Ureteral Diseases [MESH:D014515] (1024) 
 Ureteral Obstruction [MESH:D014517] (575)
 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)
 Obstetric Labor Complications [MESH:D007744] (1550) 
 Obstetric Labor, Premature [MESH:D007752] (1316)
 Prenatal Injuries [MESH:D049188] (1314) 
 Prenatal Exposure Delayed Effects [MESH:D011297] (870)
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) 
 Marfan Syndrome [MESH:D008382] (646)
 Vascular Malformations [MESH:D054079] (1098) 
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Central Nervous System Vascular Malformations [MESH:D020785] (1031) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Heart Diseases [MESH:D006331] (8614) 
 Cardiomegaly [MESH:D006332] (4081)
 Heart Arrest [MESH:D006323] (1926)
 Heart Failure [MESH:D006333] (4058)
 Arrhythmias, Cardiac [MESH:D001145] (4679) 
 Atrial Fibrillation [MESH:D001281] (1053)
 Bradycardia [MESH:D001919] (1899)
 Tachycardia [MESH:D013610] (3339) 
 Tachycardia, Ventricular [MESH:D017180] (1386) 
 Torsades de Pointes [MESH:D016171] (880)
 Cardiomyopathies [MESH:D009202] (5331) 
 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) 
 Marfan Syndrome [MESH:D008382] (646)
 Heart Valve Diseases [MESH:D006349] (3333) 
 Aortic Valve Insufficiency [MESH:D001022] (1002)
 Aortic Valve Stenosis [MESH:D001024] (1742) 
 Aortic Stenosis, Subvalvular [MESH:D001020] (1455) 
 Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)
 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 Artery Disease [MESH:D003324] (2685)
 Coronary Thrombosis [MESH:D003328] (255)
 Coronary Vasospasm [MESH:D003329] (533)
 Coronary Stenosis [MESH:D023921] (1806) 
 Coronary Restenosis [MESH:D023903] (1683)
 Myocardial Infarction [MESH:D009203] (4122) 
 Myocardial Stunning [MESH:D017682] (1816)
 Ventricular Dysfunction [MESH:D018754] (2348) 
 Ventricular Dysfunction, Left [MESH:D018487] (1631)
 Vascular Diseases [MESH:D014652] (8691) 
 Angioedema [MESH:D000799] (837)
 Arteritis [MESH:D001167] (1084)
 Compartment Syndromes [MESH:D003161] (80)
 Hemorrhoids [MESH:D006484] (166)
 Hepatic Veno-Occlusive Disease [MESH:D006504] (208)
 Retinal Vein Occlusion [MESH:D012170] (607)
 Vascular System Injuries [MESH:D057772] (2086)
 Aneurysm [MESH:D000783] (1886) 
 Aneurysm, Ruptured [MESH:D017542] (645) 
 Aortic Rupture [MESH:D001019] (637)
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
 Aortic Aneurysm, Thoracic [MESH:D017545] (781)
 Aortic Rupture [MESH:D001019] (637)
 Aortic Diseases [MESH:D001018] (1737) 
 Aortic Aneurysm [MESH:D001014] (1721) 
 Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
 Aortic Aneurysm, Thoracic [MESH:D017545] (781)
 Aortic Rupture [MESH:D001019] (637)
 Arterial Occlusive Diseases [MESH:D001157] (4520) 
 Carotid Stenosis [MESH:D016893] (174)
 Arteriosclerosis [MESH:D001161] (4466) 
 Atherosclerosis [MESH:D050197] (4188)
 Coronary Artery Disease [MESH:D003324] (2685)
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Cerebrovascular Disorders [MESH:D002561] (5541) 
 Vertebrobasilar Insufficiency [MESH:D014715] (9)
 Brain Ischemia [MESH:D002545] (4873) 
 Ischemic Attack, Transient [MESH:D002546] (1313)
 Vertebrobasilar Insufficiency [MESH:D014715] (9)
 Brain Infarction [MESH:D020520] (2571) 
 Cerebral Infarction [MESH:D002544] (2458) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Carotid Artery Diseases [MESH:D002340] (1993) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Carotid Stenosis [MESH:D016893] (174)
 Intracranial Arterial Diseases [MESH:D020765] (2468) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Cerebral Arterial Diseases [MESH:D002539] (2440) 
 Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356)
 Intracranial Hemorrhages [MESH:D020300] (3269) 
 Cerebral Hemorrhage [MESH:D002543] (2873)
 Subarachnoid Hemorrhage [MESH:D013345] (1082)
 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)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Embolism and Thrombosis [MESH:D016769] (3374) 
 Embolism [MESH:D004617] (1137) 
 Pulmonary Embolism [MESH:D011655] (1118)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356)
 Thrombosis [MESH:D013927] (3101) 
 Coronary Thrombosis [MESH:D003328] (255)
 Thromboembolism [MESH:D013923] (732) 
 Venous Thromboembolism [MESH:D054556] (400)
 Intracranial Embolism and Thrombosis [MESH:D002542] (550) 
 Carotid Artery Thrombosis [MESH:D002341] (138)
 Intracranial Thrombosis [MESH:D020767] (481) 
 Sinus Thrombosis, Intracranial [MESH:D012851] (356)
 Venous Thrombosis [MESH:D020246] (1141) 
 Retinal Vein Occlusion [MESH:D012170] (607)
 Hemostatic Disorders [MESH:D020141] (2894) 
 Multiple Myeloma [MESH:D009101] (2765)
 Hypertension [MESH:D006973] (5655) 
 Hypertension, Essential [MESH:C562386] (1308)
 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 Artery Disease [MESH:D003324] (2685)
 Coronary Thrombosis [MESH:D003328] (255)
 Coronary Vasospasm [MESH:D003329] (533)
 Coronary Stenosis [MESH:D023921] (1806) 
 Coronary Restenosis [MESH:D023903] (1683)
 Myocardial Infarction [MESH:D009203] (4151) 
 Myocardial Stunning [MESH:D017682] (1816)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Spinal Cord Vascular Diseases [MESH:D020758] (14) 
 Spinal Cord Ischemia [MESH:D020760] (12)
 Vasculitis [MESH:D014657] (2604) 
 Arteritis [MESH:D001167] (1084)
 Behcet Syndrome [MESH:D001528] (1784)
C15. Hemic and Lymphatic Diseases 
C15. Hemic and Lymphatic Diseases
 Hematologic Diseases [MESH:D006402] (6174) 
 Methemoglobinemia [MESH:D008708] (850)
 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 Coagulation Disorders [MESH:D001778] (1828) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Thrombocythemia, Essential [MESH:D013920] (707)
 Blood Coagulation Disorders, Inherited [MESH:D025861] (720) 
 Hypoprothrombinemias [MESH:D007020] (157)
 Thrombasthenia [MESH:D013915] (98)
 Coagulation Protein Disorders [MESH:D020147] (580) 
 Hypoprothrombinemias [MESH:D007020] (157)
 Purpura [MESH:D011693] (475) 
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Blood Platelet Disorders [MESH:D001791] (3174) 
 Thrombasthenia [MESH:D013915] (98)
 Thrombocytopenia [MESH:D013921] (2966) 
 Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79)
 Thrombotic Microangiopathies [MESH:D057049] (2598) 
 Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Thrombocytosis [MESH:D013922] (720) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Blood Protein Disorders [MESH:D001796] (3051) 
 Hypoproteinemia [MESH:D007019] (1335) 
 Hypoalbuminemia [MESH:D034141] (1332)
 Paraproteinemias [MESH:D010265] (2781) 
 Multiple Myeloma [MESH:D009101] (2765)
 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)
 Myeloproliferative Disorders [MESH:D009196] (1492) 
 Thrombocytosis [MESH:D013922] (720) 
 Thrombocythemia, Essential [MESH:D013920] (707)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Hemorrhagic Disorders [MESH:D006474] (3359) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Hypoprothrombinemias [MESH:D007020] (157)
 Thrombasthenia [MESH:D013915] (98)
 Thrombocythemia, Essential [MESH:D013920] (707)
 Hemostatic Disorders [MESH:D020141] (2932) 
 Multiple Myeloma [MESH:D009101] (2765)
 Leukocyte Disorders [MESH:D007960] (2662) 
 Leukostasis [MESH:D018921] (769)
 Leukopenia [MESH:D007970] (1921) 
 Agranulocytosis [MESH:D000380] (1675) 
 Neutropenia [MESH:D009503] (1629)
 Thrombophilia [MESH:D019851] (592) 
 Disseminated Intravascular Coagulation [MESH:D004211] (462)
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Lymphatic Diseases [MESH:D008206] (5167) 
 Splenic Diseases [MESH:D013158] (1323)
 Lymphoproliferative Disorders [MESH:D008232] (4638) 
 Giant Lymph Node Hyperplasia [MESH:D005871] (1013)
 Sarcoidosis [MESH:D012507] (895)
 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, 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) 
 Marfan Syndrome [MESH:D008382] (646)
 Cardiovascular Abnormalities [MESH:D018376] (3294) 
 Heart Defects, Congenital [MESH:D006330] (2611) 
 Marfan Syndrome [MESH:D008382] (646)
 Vascular Malformations [MESH:D054079] (1108) 
 Arteriovenous Malformations [MESH:D001165] (1058) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Central Nervous System Vascular Malformations [MESH:D020785] (1018) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Chromosome Disorders [MESH:D025063] (2030) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Eye Abnormalities [MESH:D005124] (1233) 
 Aniridia [MESH:D015783] (312) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Musculoskeletal Abnormalities [MESH:D009139] (3779) 
 Craniofacial Abnormalities [MESH:D019465] (3064) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Limb Deformities, Congenital [MESH:D017880] (1813) 
 Acromicric dysplasia [MESH:C535662] (520)
 Metaphyseal Anadysplasia 2 [MESH:C567771] (452)
 Nervous System Malformations [MESH:D009421] (3354) 
 Central Nervous System Vascular Malformations [MESH:D020785] (1031) 
 Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
 Neural Tube Defects [MESH:D009436] (2143) 
 Spinal Dysraphism [MESH:D016135] (1025)
 Urogenital Abnormalities [MESH:D014564] (2064) 
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Genetic Diseases, Inborn [MESH:D030342] (9766) 
 Camurati-Engelmann Syndrome [MESH:D003966] (492)
 Cystic Fibrosis [MESH:D003550] (760)
 Marfan Syndrome [MESH:D008382] (646)
 Anemia, Hemolytic, Congenital [MESH:D000745] (2001) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Anemia, Hypoplastic, Congenital [MESH:D029502] (1665) 
 Fanconi Anemia [MESH:D005199] (1604)
 Blood Coagulation Disorders, Inherited [MESH:D025861] (722) 
 Hypoprothrombinemias [MESH:D007020] (157)
 Thrombasthenia [MESH:D013915] (98)
 Chromosome Disorders [MESH:D025063] (2030) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Eye Diseases, Hereditary [MESH:D015785] (1867) 
 Aniridia [MESH:D015783] (312) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Genetic Diseases, X-Linked [MESH:D040181] (3028) 
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 Hemoglobinopathies [MESH:D006453] (1863) 
 Anemia, Sickle Cell [MESH:D000755] (1722)
 Metabolism, Inborn Errors [MESH:D008661] (6032) 
 Myeloperoxidase Deficiency [MESH:C562864] (335)
 Coumarin Resistance [MESH:C563039] (397)
 Drug Metabolism, Poor, CYP2C19-Related [MESH:C563703] (182)
 Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) 
 Hyperhomocysteinemia [MESH:D020138] (1724)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Hyperlipoproteinemia Type II [MESH:D006938] (707)
 Metal Metabolism, Inborn Errors [MESH:D008664] (2017) 
 Hemochromatosis [MESH:D006432] (1694)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027) 
 Renal Aminoacidurias [MESH:D000608] (95) 
 Cystinuria [MESH:D003555] (67) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Muscular Dystrophies [MESH:D009136] (1597) 
 Muscular Dystrophy, Duchenne [MESH:D020388] (942)
 Neoplastic Syndromes, Hereditary [MESH:D009386] (2578) 
 Li-Fraumeni Syndrome [MESH:D016864] (859)
 Wilms Tumor [MESH:D009396] (553) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Skin Diseases, Genetic [MESH:D012873] (3456) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Infant, Newborn, Diseases [MESH:D007232] (3064) 
 Cystic Fibrosis [MESH:D003550] (760)
 Thrombocytopenia, Neonatal Alloimmune [MESH:D054098] (79)
C17. Skin and Connective Tissue Diseases 
C17. Skin and Connective Tissue Diseases
 Connective Tissue Diseases [MESH:D003240] (4490) 
 Dermatomyositis [MESH:D003882] (1826)
 Marfan Syndrome [MESH:D008382] (646)
 Penile Induration [MESH:D010411] (495)
 Scleroderma, Localized [MESH:D012594] (1597)
 Collagen Diseases [MESH:D003095] (1267) 
 Keloid [MESH:D007627] (1111)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317) 
 Lupus Nephritis [MESH:D008181] (602)
 Rheumatic Diseases [MESH:D012216] (3619) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3603)
 Skin Diseases [MESH:D012871] (8774) 
 Dermatomyositis [MESH:D003882] (1826)
 Exanthema [MESH:D005076] (301)
 Keratosis [MESH:D007642] (1941)
 Scleroderma, Localized [MESH:D012594] (1597)
 Skin Neoplasms [MESH:D012878] (2991)
 Breast Diseases [MESH:D001941] (6148) 
 Breast Neoplasms [MESH:D001943] (6077)
 Dermatitis [MESH:D003872] (4530) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Drug Eruptions [MESH:D003875] (2697)
 Dermatitis, Contact [MESH:D003877] (3394) 
 Dermatitis, Allergic Contact [MESH:D017449] (3241)
 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)
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Skin Diseases, Infectious [MESH:D012874] (2684) 
 Skin Diseases, Parasitic [MESH:D012876] (2526) 
 Leishmaniasis [MESH:D007896] (2516) 
 Leishmaniasis, Cutaneous [MESH:D016773] (2359)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Lipodystrophy [MESH:D008060] (930) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Skin Diseases, Papulosquamous [MESH:D017444] (3392) 
 Lichenoid Eruptions [MESH:D017512] (1324)
 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) 
 Metabolic Syndrome X [MESH:D024821] (2151)
 Brain Diseases, Metabolic [MESH:D001928] (3350) 
 Hepatic Encephalopathy [MESH:D006501] (1795)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)
 Calcium Metabolism Disorders [MESH:D002128] (3634) 
 Hypercalcemia [MESH:D006934] (1999)
 Calcinosis [MESH:D002114] (2989) 
 Idiopathic basal ganglia calcification 1 [MESH:C536275] (139)
 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 2 [MESH:D003924] (4219)
 Hyperinsulinism [MESH:D006946] (3586) 
 Insulin Resistance [MESH:D007333] (3511) 
 Metabolic Syndrome X [MESH:D024821] (2151)
 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) 
 Hypercholesterolemia [MESH:D006937] (1404)
 Hyperlipoproteinemias [MESH:D006951] (903) 
 Hyperlipoproteinemia Type II [MESH:D006938] (707)
 Lipodystrophy [MESH:D008060] (930) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
 Malabsorption Syndromes [MESH:D008286] (1869) 
 Hyperhomocysteinemia [MESH:D020138] (1716)
 Metabolism, Inborn Errors [MESH:D008661] (6028) 
 Myeloperoxidase Deficiency [MESH:C562864] (335)
 Coumarin Resistance [MESH:C563039] (397)
 Drug Metabolism, Poor, CYP2C19-Related [MESH:C563703] (182)
 Drug Metabolism, Poor, CYP2D6-Related [MESH:C563835] (220)
 Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) 
 Hyperhomocysteinemia [MESH:D020138] (1724)
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)
 Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634) 
 Urea Cycle Disorders, Inborn [MESH:D056806] (315) 
 3-methylcrotonyl CoA carboxylase 2 deficiency [MESH:C535309] (32)
 Lipid Metabolism, Inborn Errors [MESH:D008052] (2071) 
 Hyperlipoproteinemia Type II [MESH:D006938] (707)
 Metal Metabolism, Inborn Errors [MESH:D008664] (2017) 
 Hemochromatosis [MESH:D006432] (1694)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026) 
 Renal Aminoacidurias [MESH:D000608] (89) 
 Cystinuria [MESH:D003555] (67) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Mitochondrial Diseases [MESH:D028361] (2561) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Mitochondrial Myopathies [MESH:D017240] (2176)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Proteostasis Deficiencies [MESH:D057165] (3522) 
 TDP-43 Proteinopathies [MESH:D057177] (3337) 
 Amyotrophic Lateral Sclerosis [MESH:D000690] (3296) 
 Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
 Amyotrophic Lateral Sclerosis, Sporadic [MESH:C566291] (239)
 Skin Diseases, Metabolic [MESH:D012875] (1574) 
 Lipodystrophy [MESH:D008060] (930) 
 Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490)
 Porphyrias [MESH:D011164] (917) 
 Porphyrias, Hepatic [MESH:D017094] (881) 
 Porphyria Cutanea Tarda [MESH:D017119] (766)
 Wasting Syndrome [MESH:D019282] (1959) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Water-Electrolyte Imbalance [MESH:D014883] (2790) 
 Hypercalcemia [MESH:D006934] (1999)
 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) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Obesity, Morbid [MESH:D009767] (515)
 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)
 Diabetes Mellitus [MESH:D003920] (6159) 
 Diabetes Mellitus, Experimental [MESH:D003921] (4771)
 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)
 Diabetic Angiopathies [MESH:D003925] (1984) 
 Diabetic Retinopathy [MESH:D003930] (1371)
 Endocrine Gland Neoplasms [MESH:D004701] (4925) 
 Ovarian Neoplasms [MESH:D010051] (3275)
 Pancreatic Neoplasms [MESH:D010190] (3820)
 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) 
 Disorders of Sex Development [MESH:D012734] (1637) 
 46, XY Disorders of Sex Development [MESH:D058490] (1060) 
 WAGR Syndrome [MESH:D017624] (270) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Ovarian Diseases [MESH:D010049] (4253) 
 Ovarian Neoplasms [MESH:D010051] (3281)
 Primary Ovarian Insufficiency [MESH:D016649] (270)
 Parathyroid Diseases [MESH:D010279] (1604) 
 Hyperparathyroidism [MESH:D006961] (1475) 
 Hyperparathyroidism, Secondary [MESH:D006962] (1138)
 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) 
 Glomerulonephritis, Membranoproliferative [MESH:D015432] (770)
 Autoimmune Diseases [MESH:D001327] (5067) 
 Arthritis, Juvenile [MESH:D001171] (1060)
 Arthritis, Rheumatoid [MESH:D001172] (3601)
 Glomerulonephritis, IGA [MESH:D005922] (897)
 Glomerulonephritis, Membranous [MESH:D015433] (642)
 Hepatitis, Autoimmune [MESH:D019693] (1982)
 Autoimmune Diseases of the Nervous System [MESH:D020274] (2238) 
 Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732) 
 Multiple Sclerosis [MESH:D009103] (1716)
 Lupus Erythematosus, Systemic [MESH:D008180] (2317) 
 Lupus Nephritis [MESH:D008181] (602)
 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) 
 Dermatitis, Atopic [MESH:D003876] (2052)
 Respiratory Hypersensitivity [MESH:D012130] (4250) 
 Ige Responsiveness, Atopic [MESH:C564133] (267)
 Asthma [MESH:D001249] (3914)
 Rhinitis, Allergic, Perennial [MESH:D012221] (625) 
 Allergic Rhinitis [MESH:C567078] (181)
 Urticaria [MESH:D014581] (2668) 
 Angioedema [MESH:D000799] (837)
 Immunologic Deficiency Syndromes [MESH:D007153] (3788) 
 HIV Infections [MESH:D015658] (3402) 
 HIV Wasting Syndrome [MESH:D019247] (1956)
 Immunoproliferative Disorders [MESH:D007160] (4761) 
 Lymphoproliferative Disorders [MESH:D008232] (4734) 
 Giant Lymph Node Hyperplasia [MESH:D005871] (1013)
 Multiple Myeloma [MESH:D009101] (2767)
 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, B-Cell [MESH:D016393] (2624) 
 Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
 Paraproteinemias [MESH:D010265] (2791) 
 Multiple Myeloma [MESH:D009101] (2765)
C22. Animal Diseases 
C22. Animal Diseases
 Animal Diseases [MESH:D000820] (3656) 
 Mammary Neoplasms, Animal [MESH:D015674] (2735)
 Paratuberculosis [MESH:D010283] (427)
 Cattle Diseases [MESH:D002418] (416) 
 Tuberculosis, Bovine [MESH:D014380] (380)
C23. Pathological Conditions, Signs and Symptoms 
C23. Pathological Conditions, Signs and Symptoms
 Pathological Conditions, Anatomical [MESH:D020763] (6074) 
 Atrophy [MESH:D001284] (2603)
 Plaque, Atherosclerotic [MESH:D058226] (696)
 Ventricular Remodeling [MESH:D020257] (686)
 Hernia [MESH:D006547] (2825) 
 Hernia, Diaphragmatic [MESH:D006548] (2647)
 Intervertebral Disc Displacement [MESH:D007405] (520) 
 Intervertebral disc disease [MESH:C535531] (514)
 Hypertrophy [MESH:D006984] (4476) 
 Cardiomegaly [MESH:D006332] (3802)
 Hepatomegaly [MESH:D006529] (1169)
 Splenomegaly [MESH:D013163] (1258)
 Pathologic Processes [MESH:D010335] (9863) 
 Emphysema [MESH:D004646] (1096)
 Gliosis [MESH:D005911] (1419)
 Growth Disorders [MESH:D006130] (2438)
 Hyperbilirubinemia [MESH:D006932] (1860)
 Hyperplasia [MESH:D006965] (2463)
 Intraoperative Complications [MESH:D007431] (131)
 Ischemia [MESH:D007511] (3049)
 Metaplasia [MESH:D008679] (1469)
 Necrosis [MESH:D009336] (4019)
 Neointima [MESH:D058426] (814)
 Nerve Degeneration [MESH:D009410] (4061)
 Arrhythmias, Cardiac [MESH:D001145] (4658) 
 Atrial Fibrillation [MESH:D001281] (1053)
 Bradycardia [MESH:D001919] (1899)
 Tachycardia [MESH:D013610] (3339) 
 Tachycardia, Ventricular [MESH:D017180] (1386) 
 Torsades de Pointes [MESH:D016171] (880)
 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)
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Disease Attributes [MESH:D020969] (3654) 
 Disease Progression [MESH:D018450] (2868)
 Fibrosis [MESH:D005355] (3133) 
 Peritoneal Fibrosis [MESH:D056627] (488)
 Cicatrix [MESH:D002921] (1115) 
 Keloid [MESH:D007627] (1110)
 Hemorrhage [MESH:D006470] (4451) 
 Postoperative Hemorrhage [MESH:D019106] (16)
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Gastrointestinal Hemorrhage [MESH:D006471] (815) 
 Peptic Ulcer Hemorrhage [MESH:D010438] (553)
 Hematoma [MESH:D006406] (281) 
 Hematoma, Subdural [MESH:D006408] (215)
 Intracranial Hemorrhages [MESH:D020300] (3241) 
 Cerebral Hemorrhage [MESH:D002543] (2872)
 Hematoma, Subdural [MESH:D006408] (212)
 Subarachnoid Hemorrhage [MESH:D013345] (1081)
 Purpura [MESH:D011693] (475) 
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Inflammation [MESH:D007249] (5241) 
 Neurogenic Inflammation [MESH:D020078] (2246)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (3563) 
 Sepsis [MESH:D018805] (3562) 
 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)
 Postoperative Hemorrhage [MESH:D019106] (16)
 Reperfusion Injury [MESH:D015427] (4968) 
 Myocardial Reperfusion Injury [MESH:D015428] (3500)
 Shock [MESH:D012769] (2550) 
 Multiple Organ Failure [MESH:D009102] (1836)
 Shock, Hemorrhagic [MESH:D012771] (2042)
 Systemic Inflammatory Response Syndrome [MESH:D018746] (1832) 
 Shock, Septic [MESH:D012772] (1830)
 Signs and Symptoms [MESH:D012816] (10659) 
 Edema [MESH:D004487] (3726)
 Body Temperature Changes [MESH:D001832] (3130) 
 Fever [MESH:D005334] (2856)
 Hypothermia [MESH:D007035] (2075)
 Body Weight [MESH:D001835] (4972) 
 Birth Weight [MESH:D001724] (377)
 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) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
 Obesity, Morbid [MESH:D009767] (515)
 Neurologic Manifestations [MESH:D009461] (8702) 
 Seizures [MESH:D012640] (4502)
 Dyskinesias [MESH:D020820] (3285) 
 Dystonia [MESH:D004421] (848)
 Tremor [MESH:D014202] (840)
 Neurobehavioral Manifestations [MESH:D019954] (4706) 
 Consciousness Disorders [MESH:D003244] (677) 
 Unconsciousness [MESH:D014474] (657) 
 Coma [MESH:D003128] (492)
 Syncope [MESH:D013575] (128)
 Memory Disorders [MESH:D008569] (3233) 
 Amnesia [MESH:D000647] (1911)
 Intellectual Disability [MESH:D008607] (1476) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Perceptual Disorders [MESH:D010468] (343) 
 Hallucinations [MESH:D006212] (251)
 Neuromuscular Manifestations [MESH:D020879] (2130) 
 Muscle Hypertonia [MESH:D009122] (775) 
 Muscle Rigidity [MESH:D009127] (617)
 Muscle Hypotonia [MESH:D009123] (258) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Pain [MESH:D010146] (3869) 
 Headache [MESH:D006261] (1417)
 Neuralgia [MESH:D009437] (2074)
 Sensation Disorders [MESH:D012678] (5009) 
 Hearing Disorders [MESH:D006311] (2101) 
 Hearing Loss [MESH:D034381] (2066) 
 Deafness [MESH:D003638] (593)
 Somatosensory Disorders [MESH:D020886] (4000) 
 Hyperalgesia [MESH:D006930] (3929)
 Hypesthesia [MESH:D006987] (58)
 Taste Disorders [MESH:D013651] (461) 
 Ageusia [MESH:D000370] (20)
 Pain [MESH:D010146] (4511) 
 Headache [MESH:D006261] (1417)
 Neuralgia [MESH:D009437] (2074)
 Pain, Postoperative [MESH:D010149] (529)
 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) 
 Constipation [MESH:D003248] (506)
 Nausea [MESH:D009325] (2300)
 Vomiting [MESH:D014839] (1354)
 Signs and Symptoms, Respiratory [MESH:D012818] (2724) 
 Anoxia [MESH:D000860] (1698)
 Dyspnea [MESH:D004417] (248)
 Respiratory Sounds [MESH:D012135] (713)
 Hypoventilation [MESH:D007040] (359) 
 Congenital central hypoventilation syndrome [MESH:C536209] (341)
 Skin Manifestations [MESH:D012877] (1250) 
 Purpura [MESH:D011693] (475) 
 Purpura, Thrombocytopenic [MESH:D011696] (237) 
 Purpura, Thrombotic Thrombocytopenic [MESH:D011697] (222)
 Urological Manifestations [MESH:D020924] (3532) 
 Proteinuria [MESH:D011507] (3293) 
 Albuminuria [MESH:D000419] (2394)
C24. Occupational Diseases 
C24. Occupational Diseases
 Z. Exceptions (1530) 
 Not Fully Specified [NFS] (1530)
 Occupational Diseases [MESH:D009784] (3402) 
 Agricultural Workers' Diseases [MESH:D000382] (193)
 Persian Gulf Syndrome [MESH:D018923] (166)
 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-Induced Liver Injury [MESH:D056486] (4936)
 Drug Hypersensitivity [MESH:D004342] (4001) 
 Drug Eruptions [MESH:D003875] (2697)
 Poisoning [MESH:D011041] (6703) 
 Arsenic Poisoning [MESH:D020261] (2540)
 Drug-Induced Liver Injury [MESH:D056486] (4936)
 Lead Poisoning [MESH:D007855] (515)
 Manganese Poisoning [MESH:D020149] (2214)
 Neurotoxicity Syndromes [MESH:D020258] (3323)
 Organophosphate Poisoning [MESH:D062025] (497)
 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)
 Tobacco Use Disorder [MESH:D014029] (628)
 Alcohol-Related Disorders [MESH:D019973] (3869) 
 Alcohol-Induced Disorders [MESH:D020751] (3350) 
 Liver Diseases, Alcoholic [MESH:D008108] (3243) 
 Hepatitis, Alcoholic [MESH:D006519] (1613)
 Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
 Opioid-Related Disorders [MESH:D009293] (1491) 
 Heroin Dependence [MESH:D006556] (950)
 Morphine Dependence [MESH:D009021] (855)
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)
 Fractures, Bone [MESH:D050723] (597) 
 Hip Fractures [MESH:D006620] (81)
 Femoral Fractures [MESH:D005264] (137) 
 Hip Fractures [MESH:D006620] (82)
 Hip Injuries [MESH:D025981] (83) 
 Hip Fractures [MESH:D006620] (81)
 Leg Injuries [MESH:D007869] (152) 
 Femoral Fractures [MESH:D005264] (137) 
 Hip Fractures [MESH:D006620] (82)
 Radiation Injuries [MESH:D011832] (2718) 
 Radiation Injuries, Experimental [MESH:D011833] (2662)
 Rupture [MESH:D012421] (646) 
 Aortic Rupture [MESH:D001019] (637)
 Spinal Cord Injuries [MESH:D013119] (2688) 
 Spinal Cord Compression [MESH:D013117] (1800)
 Thoracic Injuries [MESH:D013898] (1831) 
 Lung Injury [MESH:D055370] (1814)
 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) 
 Sulfur Compounds [MESH:D013457] (10450) 
 Thiophenes [MESH:D013876] (883) 
 Thienopyridines [MESH:D058924] (24) 
 Ticlopidine [MESH:D013988] (8)
D03. Heterocyclic Compounds 
D03. Heterocyclic Compounds
 Heterocyclic Compounds [MESH:D006571] (56330) 
 Heterocyclic Compounds, 1-Ring [MESH:D006573] (30631) 
 Pyridines [MESH:D011725] (4775) 
 Thienopyridines [MESH:D058924] (24) 
 Ticlopidine [MESH:D013988] (8)
 Thiophenes [MESH:D013876] (844) 
 Thienopyridines [MESH:D058924] (24) 
 Ticlopidine [MESH:D013988] (8)
 Heterocyclic Compounds, 2-Ring [MESH:D006574] (24204) 
 Thienopyridines [MESH:D058924] (24) 
 Ticlopidine [MESH:D013988] (8)
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment 
E. Analytical, Diagnostic and Therapeutic Techniques and Equipment
 Diagnosis [MESH:D003933] (1924) 
 Diagnostic Techniques and Procedures [MESH:D019937] (1902) 
 Physical Examination [MESH:D010808] (1041) 
 Body Constitution [MESH:D001824] (450) 
 Body Weights and Measures [MESH:D001837] (448) 
 Body Size [MESH:D049628] (439) 
 Body Weight [MESH:D001835] (433) 
 Overweight [MESH:D050177] (428) 
 Obesity [MESH:D009765] (427) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)
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) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Mental Disorders [MESH:D001523] (2063) 
 Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245) 
 Intellectual Disability [MESH:D008607] (1109) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
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)
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 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)
 Chromosomes, Human, 21-22 and Y [MESH:D002904] (294) 
 Chromosomes, Human, Pair 21 [MESH:D002891] (58) 
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 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)
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Chromosome Aberrations [MESH:D002869] (1297) 
 Aneuploidy [MESH:D000782] (1220) 
 Monosomy [MESH:D009006] (1121) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Sequence Deletion [MESH:D017384] (1120) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Ploidies [MESH:D011003] (1227) 
 Aneuploidy [MESH:D000782] (1220) 
 Monosomy [MESH:D009006] (1121) 
 Chromosome Deletion [MESH:D002872] (1117) 
 Chromosome 17 deletion [MESH:C538045] (769)
 Hypotonia-Cystinuria Syndrome [MESH:C564710] (52)
 Physiological Phenomena [MESH:D010829] (788) 
 Body Constitution [MESH:D001824] (453) 
 Body Weights and Measures [MESH:D001837] (444) 
 Body Size [MESH:D049628] (438) 
 Body Weight [MESH:D001835] (433) 
 Overweight [MESH:D050177] (428) 
 Obesity [MESH:D009765] (427) 
 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome [MESH:C567292] (232)