Item 2 of 260 (back to results) previous next   uranyl acetate C005460               MeSH Unique Identifier: C005460 Scope Notes: Used after fixation in uranaffin procedure Chemical – Gene Interaction Note 1: Uranyl acetate affects the expression of AADAT mRNA Note 2: Uranyl acetate affects the expression of AANAT mRNA Click here for more information

Current search: C04. Neoplasms: Neoplasms [MESH:D009369] > Neoplastic Syndromes, Hereditary [MESH:D009386] > Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  A-kinase anchor proteins [HGNC:AKAP] (99)   A kinase (PRKA) anchor protein 01 [HGNC:AKAP1] (11)  Aldo-keto reductases [HGNC:AKR] (282)   aldo-keto reductase family 1, member C3 [HGNC:AKR1C3] (128)  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   notch 2 [HGNC:NOTCH2] (18)  Ataxins [HGNC:ATXN] (46)   ataxin 10 [HGNC:ATXN10] (4)  ATP-binding cassette transporters [HGNC:ABC] (821)   ATP-binding cassette transporters, subfamily C [HGNC:ABCC] (458)   ATP-binding cassette, sub-family C (CFTR/MRP), member 8 [HGNC:ABCC8] (11)  Basic helix-loop-helix [HGNC:BHLH] (618)   inhibitor of DNA binding 2, dominant negative helix-loop-helix protein [HGNC:ID2] (69)  CD molecules [HGNC:CD] (1459)   5'-nucleotidase, ecto (CD73) [HGNC:NT5E] (24)  lysosomal-associated membrane protein 2 [HGNC:LAMP2] (21)  tumor necrosis factor receptor superfamily, member 01B [HGNC:TNFRSF1B] (49)  Components of oligomeric golgi complex [HGNC:COG] (23)   component of oligomeric golgi complex 7 [HGNC:COG7] (6)  EF-hand domain containing [HGNC:EFHAND] (226)   multiple coagulation factor deficiency 2 [HGNC:MCFD2] (8)  Endogenous Ligands [HGNC:ENDOLIG] (1191)   chorionic gonadotropin, beta polypeptide [HGNC:CGB] (67)  F-boxes [HGNC:FBX] (66)   F-boxes and leucine-rich repeats [HGNC:FBXL] (58)   lysine (K)-specific demethylase 2B [HGNC:KDM2B] (12)  High mobility group [HGNC:HMG] (101)   High mobility group, Canonical [HGNC:HMG] (98)   high mobility group box 1 [HGNC:HMGB1] (48)  Histocompatibility complex [HGNC:HLA] (108)   major histocompatibility complex, class I, E [HGNC:HLA-E] (29)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   C1-set domain containing [HGNC:C1SET] (121)   major histocompatibility complex, class I, E [HGNC:HLA-E] (29)  Intermediate filaments [HGNC:IF] (273)   Type IV [HGNC:] (57)   neurofilament, light polypeptide [HGNC:NEFL] (22)  IP3 receptors [HGNC:ITPR] (60)   inositol 1,4,5-trisphosphate receptor, type 1 [HGNC:ITPR1] (44)  inositol 1,4,5-trisphosphate receptor, type 2 [HGNC:ITPR2] (18)  K-demethylases [HGNC:KDM] (47)   lysine (K)-specific demethylase 2B [HGNC:KDM2B] (12)  lysine (K)-specific demethylase 4B [HGNC:KDM4B] (21)  Kinesins [HGNC:KIF] (68)   kinesin family member 01B [HGNC:KIF1B] (18)  kinesin family member 03C [HGNC:KIF3C] (10)  PHD-type zinc fingers [HGNC:PHF] (103)   myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10 [HGNC:MLLT10] (11)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   kinesin family member 01B [HGNC:KIF1B] (18)  Proteasome (prosome, macropain) subunits [HGNC:PSM] (98)   proteasome (prosome, macropain) subunit, alpha type, 4 [HGNC:PSMA4] (12)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase, catalytic subunits [HGNC:PPP] (49)   protein phosphatase 2, catalytic subunit, alpha isozyme [HGNC:PPP2CA] (20)  Protein phosphatase 1, regulatory subunits [HGNC:PPP1R] (155)   protein tyrosine kinase 2 [HGNC:PTK2] (77)  Receptor accessory proteins [HGNC:REEP] (11)   receptor accessory protein 1 [HGNC:REEP1] (11)  RNA binding motif containing [HGNC:RRM] (251)   RNA binding motif (RNP1, RRM) protein 3 [HGNC:RBM3] (16)  RNA binding motif protein 08A [HGNC:RBM8A] (11)  L ribosomal proteins [HGNC:RPL] (79)   ribosomal protein L15 [HGNC:RPL15] (8)  Serine/threonine phosphatases [HGNC:PPP-PPM-CTD] (43)   A kinase (PRKA) anchor protein 01 [HGNC:AKAP1] (11)  SH2 domain containing [HGNC:SH2D] (431)   phosphoinositide-3-kinase, regulatory subunit 1 (alpha) [HGNC:PIK3R1] (44)  Solute carriers [HGNC:SLC] (716)   solute carrier family 02 (facilitated glucose transporter), member 03 [HGNC:SLC2A3] (76)  Syndecans (transmembrane HSPG) [HGNC:SDC] (36)   syndecan 3 [HGNC:SDC3] (8)  Tubulins [HGNC:TUB] (87)   tubulin, alpha 1a [HGNC:TUBA1A] (28)  Tudor domain containing [HGNC:TDRD] (64)   A kinase (PRKA) anchor protein 01 [HGNC:AKAP1] (11)  lysine (K)-specific demethylase 4B [HGNC:KDM4B] (21)  Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295)   tumor necrosis factor receptor superfamily, member 01B [HGNC:TNFRSF1B] (49)  Voltage-dependent anion channels [HGNC:VDAC] (33)   voltage-dependent anion channel 2 [HGNC:VDAC2] (16) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   expression (494)  Increases (5571)   expression (3238) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Extremities [MESH:D005121] (484)   Upper Extremity [MESH:D034941] (441)   Hand [MESH:D006225] (428)   Fingers [MESH:D005385] (422)   Cohen syndrome [MESH:C536438] (21)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Radius [MESH:D011884] (126)   Absent radii and thrombocytopenia [MESH:C536940] (25) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Negative Bacterial Infections [MESH:D016905] (3085)   Mycoplasmatales Infections [MESH:D009180] (1949)   Mycoplasma Infections [MESH:D009175] (1947)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Papillomavirus Infections [MESH:D030361] (630)  Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  RNA Virus Infections [MESH:D012327] (4215)   Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Opportunistic Infections [MESH:D009894] (949)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Cysts [MESH:D003560] (2625)   Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Neoplasms by Histologic Type [MESH:D009370] (8793)   Leukemia [MESH:D007938] (4576)   Leukemia, Lymphoid [MESH:D007945] (3047)   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)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Fibroma [MESH:D005350] (1578)   Fibromatosis, Abdominal [MESH:D018221] (56)  Fibromatosis, Aggressive [MESH:D018222] (1562)   Desmoid disease, hereditary [MESH:C535944] (58)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Adenomatous Polyps [MESH:D018256] (1571)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma, Clear Cell [MESH:D018262] (1291)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Carcinoma, Squamous Cell [MESH:D002294] (4294)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Bowen's Disease [MESH:D001913] (247)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Meningioma [MESH:D008579] (978)  Nerve Sheath Neoplasms [MESH:D018317] (365)   Neurofibroma [MESH:D009455] (177)   Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Meningioma [MESH:D008579] (978)  Sarcoma, Kaposi [MESH:D012514] (1578)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Soft Tissue Neoplasms [MESH:D012983] (2003)  Abdominal Neoplasms [MESH:D000008] (74)   Desmoid disease, hereditary [MESH:C535944] (58)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5358)   Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  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)   Turcot syndrome [MESH:C536928] (159)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Skin Neoplasms [MESH:D012878] (2992)   Sebaceous Gland Neoplasms [MESH:D012626] (154)   Muir-Torre Syndrome [MESH:D055653] (102)  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)  Urogenital Neoplasms [MESH:D014565] (7002)   Genital Neoplasms, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Genital Neoplasms, Male [MESH:D005834] (6224)   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)  Tumor Virus Infections [MESH:D014412] (697)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Turcot syndrome [MESH:C536928] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Lynch Syndrome II [MESH:D055847] (103)   Muir-Torre Syndrome [MESH:D055653] (102)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Precancerous Conditions [MESH:D011230] (2858)   Aberrant Crypt Foci [MESH:D058739] (326)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Developmental [MESH:D001848] (3315)   Dysostoses [MESH:D004413] (1019)  Osteochondrodysplasias [MESH:D010009] (2440)  Acro-Osteolysis [MESH:D030981] (548)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)  Bone Resorption [MESH:D001862] (2352)   Osteolysis [MESH:D010014] (1787)   Acro-Osteolysis [MESH:D030981] (548)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Joint Diseases [MESH:D007592] (4657)   Calcification of Joints and Arteries [MESH:C565891] (60)  Arthritis [MESH:D001168] (4416)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Arthrogryposis [MESH:D001176] (329)   Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Muscular Diseases [MESH:D009135] (4071)   Arthrogryposis [MESH:D001176] (329)   Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Rhabdomyolysis [MESH:D012206] (465)   Myoglobinuria [MESH:D009212] (96)   Myoglobinuria, Acute Recurrent, Autosomal Recessive [MESH:C564832] (64)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Arthrogryposis [MESH:D001176] (329)   Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Craniofacial Abnormalities [MESH:D019465] (3098)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Microcephaly [MESH:D008831] (700)   Cohen syndrome [MESH:C536438] (21)  Limb Deformities, Congenital [MESH:D017880] (1813)   Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Absent radii and thrombocytopenia [MESH:C536940] (25)  Rheumatic Diseases [MESH:D012216] (4032)   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)   Alagille Syndrome [MESH:D016738] (105)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Liver Neoplasms [MESH:D008113] (6048)   Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Intestinal Diseases [MESH:D007410] (6206)   Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Turcot syndrome [MESH:C536928] (159)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Intestinal Neoplasms [MESH:D007414] (5359)   Colorectal Neoplasms [MESH:D015179] (5294)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Colonic Neoplasms [MESH:D003110] (4405)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Intestinal Polyposis [MESH:D044483] (1610)   Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)   Turcot syndrome [MESH:C536928] (159)  Rectal Neoplasms [MESH:D012004] (717)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Liver Diseases [MESH:D008107] (8167)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Cholestasis, Intrahepatic [MESH:D002780] (1510)   Alagille Syndrome [MESH:D016738] (105)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Liver Cirrhosis [MESH:D008103] (5542)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)  Liver Cirrhosis, Experimental [MESH:D008106] (4589)  Liver Diseases, Alcoholic [MESH:D008108] (3243)   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)   Congenital Hyperinsulinism [MESH:D044903] (132)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Mouth Diseases [MESH:D009059] (4783)   Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Lung Diseases [MESH:D008171] (7249)   Pneumonia [MESH:D011014] (3482)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Lung Neoplasms [MESH:D008175] (6012)   Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Respiration Disorders [MESH:D012120] (2218)   Apnea [MESH:D001049] (748)   Sleep Apnea Syndromes [MESH:D012891] (570)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Pneumonia [MESH:D011014] (3482)  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) 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) 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)   Aicardi-Goutieres syndrome [MESH:C535607] (57)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Hypoxia, Brain [MESH:D002534] (134)  Leukoencephalopathies [MESH:D056784] (1916)  Basal Ganglia Diseases [MESH:D001480] (4268)   Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Cerebrovascular Disorders [MESH:D002561] (5542)   Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  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)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Dementia [MESH:D003704] (4498)   Alzheimer Disease [MESH:D000544] (4275)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Frontal Lobe [MESH:D017034] (172)   Epilepsy, Nocturnal Frontal Lobe, Type 3 [MESH:C565334] (106)  Epilepsy, Generalized [MESH:D004829] (1431)   Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Movement Disorders [MESH:D009069] (4823)   Dystonic Disorders [MESH:D020821] (729)   Juvenile-onset dystonia [MESH:C537704] (143)  Parkinsonian Disorders [MESH:D020734] (4009)   Parkinson Disease [MESH:D010300] (3595)  Spinal Cord Diseases [MESH:D013118] (4376)   Spinal Cord Injuries [MESH:D013119] (1674)  Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Chronobiology Disorders [MESH:D021081] (970)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Multiple Sclerosis [MESH:D009103] (1716)  Nervous System Malformations [MESH:D009421] (3354)   Aicardi-Goutieres syndrome [MESH:C535607] (57)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)  Neuronal Migration Disorders [MESH:D054081] (264)  Microcephaly [MESH:D008831] (700)   Cohen syndrome [MESH:C536438] (21)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Turcot syndrome [MESH:C536928] (159)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neurodegenerative Diseases [MESH:D019636] (6613)   Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Ataxia 10 [MESH:C566874] (24)  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)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Cohen syndrome [MESH:C536438] (21)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Fragile X Syndrome [MESH:D005600] (353)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Neuromuscular Manifestations [MESH:D020879] (2130)   Fasciculation [MESH:D005207] (204)  Muscle Hypotonia [MESH:D009123] (258)   Cohen syndrome [MESH:C536438] (21)  Spasm [MESH:D013035] (418)   Trismus [MESH:D014313] (221)  Sensation Disorders [MESH:D012678] (5011)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Diabetic Neuropathies [MESH:D003929] (2442)  Neurofibromatosis 1 [MESH:D009456] (117)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (94)  Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Sleep Apnea Syndromes [MESH:D012891] (570)  Trauma, Nervous System [MESH:D020196] (3997)   Spinal Cord Injuries [MESH:D013119] (1676)  Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Cerulean cataract [MESH:C537955] (14)  Cataract, Coppock-Like [MESH:C565133] (20)  Refractive Errors [MESH:D012030] (457)   Myopia [MESH:D009216] (349)   Cohen syndrome [MESH:C536438] (21)  Retinal Diseases [MESH:D012164] (3747)   Retinal Degeneration [MESH:D012162] (2386)  Retinal Detachment [MESH:D012163] (1639)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Azoospermia [MESH:D053713] (1052)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   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)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293) 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)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Uterine Diseases [MESH:D014591] (2479)   Uterine Cervical Diseases [MESH:D002577] (988)   Uterine Cervical Neoplasms [MESH:D002583] (978)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Uterine Cervical Neoplasms [MESH:D002583] (978)  Urogenital Neoplasms [MESH:D014565] (5792)   Genital Neoplasms, Female [MESH:D005833] (3810)   Ovarian Neoplasms [MESH:D010051] (3281)  Uterine Neoplasms [MESH:D014594] (2433)   Endometrial Neoplasms [MESH:D016889] (1989)  Uterine Cervical Neoplasms [MESH:D002583] (978)  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)  Kidney Neoplasms [MESH:D007680] (3966)   Carcinoma, Renal Cell [MESH:D002292] (2975)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Proteinuria [MESH:D011507] (3293)  Pregnancy Complications [MESH:D011248] (4768)   Prenatal Injuries [MESH:D049188] (1314)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Alagille Syndrome [MESH:D016738] (105)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Heart Valve Diseases [MESH:D006349] (3333)  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)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Myocardial Ischemia [MESH:D017202] (5787)   Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vascular Diseases [MESH:D014652] (8691)   Calcification of Joints and Arteries [MESH:C565891] (60)  Hypertension [MESH:D006973] (5655)  Cerebrovascular Disorders [MESH:D002561] (5541)   Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  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)   Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Myocardial Ischemia [MESH:D017202] (5791)   Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Absent radii and thrombocytopenia [MESH:C536940] (25)  Blood Protein Disorders [MESH:D001796] (3051)   Hypergammaglobulinemia [MESH:D006942] (137)  Hypoproteinemia [MESH:D007019] (1335)   Hypoalbuminemia [MESH:D034141] (1332)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Hemorrhagic Disorders [MESH:D006474] (3359)   Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Lymphatic Diseases [MESH:D008206] (5167)   Lymphoproliferative Disorders [MESH:D008232] (4638)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1204)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) 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)   Bamforth syndrome [MESH:C537901] (186)  Alagille Syndrome [MESH:D016738] (105)  Bloom Syndrome [MESH:D001816] (107)  Down Syndrome [MESH:D004314] (1287)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Alagille Syndrome [MESH:D016738] (105)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Hajdu-Cheney Syndrome [MESH:D031845] (42)  Arthrogryposis [MESH:D001176] (329)   Lethal Congenital Contracture Syndrome 2 [MESH:C564369] (85)  Craniofacial Abnormalities [MESH:D019465] (3064)   Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Microcephaly [MESH:D008831] (700)   Cohen syndrome [MESH:C536438] (21)  Limb Deformities, Congenital [MESH:D017880] (1813)   Upper Extremity Deformities, Congenital [MESH:D038062] (44)   Absent radii and thrombocytopenia [MESH:C536940] (25)  Nervous System Malformations [MESH:D009421] (3354)   Aicardi-Goutieres syndrome [MESH:C535607] (57)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)  Neuronal Migration Disorders [MESH:D054081] (264)  Microcephaly [MESH:D008831] (700)   Cohen syndrome [MESH:C536438] (21)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)   Bamforth syndrome [MESH:C537901] (186)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Alagille Syndrome [MESH:D016738] (105)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Hajdu-Cheney Syndrome [MESH:D031845] (42)  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)   Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Fragile X Syndrome [MESH:D005600] (353)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 1F [MESH:C537987] (89)  Charcot-Marie-Tooth disease, Type 2E [MESH:C537994] (89)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic Paraplegia 31, Autosomal Dominant [MESH:C565210] (20)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Fragile X Syndrome [MESH:D005600] (353)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Metabolism, Inborn Errors [MESH:D008661] (6032)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Butyrylcholinesterase deficiency [MESH:C537417] (176)  Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutamine deficiency, congenital [MESH:C536832] (117)  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)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Transaldolase Deficiency [MESH:C563207] (61)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2E [MESH:C535754] (10)  Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Turcot syndrome [MESH:C536928] (159)  Adenomatous Polyposis Coli [MESH:D011125] (1565)   Desmoid disease, hereditary [MESH:C535944] (58)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Lynch Syndrome II [MESH:D055847] (103)   Muir-Torre Syndrome [MESH:D055653] (102)  Neurofibromatoses [MESH:D017253] (146)   Neurofibromatosis 1 [MESH:D009456] (117)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Diabetes Mellitus, Transient Neonatal, 2 [MESH:C563672] (42)  Congenital Hyperinsulinism [MESH:D044903] (132) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   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)  Hair Diseases [MESH:D006201] (1891)   Bamforth syndrome [MESH:C537901] (186)  Pigmentation Disorders [MESH:D010859] (1215)   Dyschromatosis symmetrica hereditaria 1 [MESH:C535729] (23)  Cafe-au-Lait Spots [MESH:D019080] (186)   Cafe au lait spots, multiple [MESH:C537421] (102)  Sebaceous Gland Diseases [MESH:D012625] (245)   Sebaceous Gland Neoplasms [MESH:D012626] (154)   Muir-Torre Syndrome [MESH:D055653] (102)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Muir-Torre Syndrome [MESH:D055653] (102)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Parapsoriasis [MESH:D010267] (49)  Skin Neoplasms [MESH:D012878] (2991)   Sebaceous Gland Neoplasms [MESH:D012626] (154)   Muir-Torre Syndrome [MESH:D055653] (102) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)   Calcification of Joints and Arteries [MESH:C565891] (60)  DNA Repair-Deficiency Disorders [MESH:D049914] (2245)   Bloom Syndrome [MESH:D001816] (107)  Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258)   Lynch syndrome I (site-specific colonic cancer) [MESH:C537261] (130)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Transient Neonatal, 2 [MESH:C563672] (42)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Congenital Hyperinsulinism [MESH:D044903] (132)  Insulin Resistance [MESH:D007333] (3511)  Hypoglycemia [MESH:D007003] (2420)   Hypoglycemia, leucine-induced [MESH:C537150] (43)  Hyperinsulinemic Hypoglycemia, Familial, 4 [MESH:C566493] (80)  Congenital Hyperinsulinism [MESH:D044903] (132)  Lipid Metabolism Disorders [MESH:D052439] (3225)   Dyslipidemias [MESH:D050171] (2428)   Hyperlipidemias [MESH:D006949] (1908)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Metabolism, Inborn Errors [MESH:D008661] (6028)   3-Hydroxyacyl-CoA Dehydrogenase Deficiency [MESH:C535310] (80)  Butyrylcholinesterase deficiency [MESH:C537417] (176)  Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutamine deficiency, congenital [MESH:C536832] (117)  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)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Transaldolase Deficiency [MESH:C563207] (61)  Congenital Disorders of Glycosylation [MESH:D018981] (188)   Congenital disorder of glycosylation type 2E [MESH:C535754] (10)  Glycogen Storage Disease [MESH:D006008] (530)   Lactate dehydrogenase deficiency type A [MESH:C538133] (119)  Glycogen Storage Disease Type IIb [MESH:D052120] (52)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  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)  Nutrition Disorders [MESH:D009748] (4945)   Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462)   Cohen syndrome [MESH:C536438] (21) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321)  Diabetes Mellitus, Transient Neonatal, 2 [MESH:C563672] (42)  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 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)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gonadal Disorders [MESH:D006058] (5088)   Hypogonadism [MESH:D007006] (1123)  Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Thyroid Diseases [MESH:D013959] (2808)   Hyperthyroidism [MESH:D006980] (1191)  Hypothyroidism [MESH:D007037] (496)   Bamforth syndrome [MESH:C537901] (186) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Aicardi-Goutieres syndrome [MESH:C535607] (57)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Multiple Sclerosis [MESH:D009103] (1716)  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)   Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)   AIDS-Related Opportunistic Infections [MESH:D017088] (944)   AIDS-related Kaposi sarcoma [MESH:C554498] (914)  Immunoproliferative Disorders [MESH:D007160] (4761)   Hypergammaglobulinemia [MESH:D006942] (137)  Lymphoproliferative Disorders [MESH:D008232] (4734)   Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704)  Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Follicular [MESH:D008224] (1025)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Paraproteinemias [MESH:D010265] (2791)   Multiple Myeloma [MESH:D009101] (2765) C22. Animal Diseases  C22. Animal Diseases  Animal Diseases [MESH:D000820] (3656)   Disease Models, Animal [MESH:D004195] (2058)  Mammary Neoplasms, Animal [MESH:D015674] (2735) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Plaque, Amyloid [MESH:D058225] (334)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Ischemia [MESH:D007511] (3049)  Metaplasia [MESH:D008679] (1469)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Tachycardia [MESH:D013610] (3339)  Death [MESH:D003643] (1328)   Death, Sudden [MESH:D003645] (725)   Sudden Infant Death [MESH:D013398] (268)  Fetal Death [MESH:D005313] (464)   Fetal Resorption [MESH:D005327] (302)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Fibrosis [MESH:D005355] (3133)   Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Hemorrhage [MESH:D006470] (4451)   Intracranial Hemorrhages [MESH:D020300] (3241)   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)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Metastasis [MESH:D009362] (4441)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Signs and Symptoms [MESH:D012816] (10659)   Edema [MESH:D004487] (3726)  Hypergammaglobulinemia [MESH:D006942] (105)  Body Temperature Changes [MESH:D001832] (3130)   Hypothermia [MESH:D007035] (2075)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)   Cohen syndrome [MESH:C536438] (21)  Neurologic Manifestations [MESH:D009461] (8702)   Paralysis [MESH:D010243] (2298)  Paresis [MESH:D010291] (419)  Seizures [MESH:D012640] (4502)  Sleep Disorders [MESH:D012893] (1301)  Dyskinesias [MESH:D020820] (3285)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Cohen syndrome [MESH:C536438] (21)  Neuromuscular Manifestations [MESH:D020879] (2130)   Fasciculation [MESH:D005207] (204)  Muscle Hypotonia [MESH:D009123] (258)   Cohen syndrome [MESH:C536438] (21)  Spasm [MESH:D013035] (418)   Trismus [MESH:D014313] (221)  Sensation Disorders [MESH:D012678] (5009)   Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sensorineural [MESH:D006319] (1227)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Apnea [MESH:D001049] (415)  Skin Manifestations [MESH:D012877] (1250)   Cafe-au-Lait Spots [MESH:D019080] (186)   Cafe au lait spots, multiple [MESH:C537421] (102)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (93) 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)  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)  Phencyclidine Abuse [MESH:D010623] (288)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243)   Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) C26. Wounds and Injuries  C26. Wounds and Injuries  Wounds and Injuries [MESH:D014947] (5171)   Fractures, Bone [MESH:D050723] (597)  Heat Stress Disorders [MESH:D018882] (226)  Spinal Cord Injuries [MESH:D013119] (2688)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Organometallic Compounds [MESH:D009942] (4369) D27. Chemical Actions and Uses  D27. Chemical Actions and Uses  Specialty Uses of Chemicals [MESH:D020313] (713)   Coloring Agents [MESH:D004396] (104)  Laboratory Chemicals [MESH:D019995] (233)   Coloring Agents [MESH:D004396] (93) 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)   Cohen syndrome [MESH:C536438] (21) 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)   Cohen syndrome [MESH:C536438] (21)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Developmental Disabilities [MESH:D002658] (151)   Cohen syndrome [MESH:C536438] (21)  Intellectual Disability [MESH:D008607] (1109)   Cohen syndrome [MESH:C536438] (21) G. Phenomena and Processes  G. Phenomena and Processes  Chemical Phenomena [MESH:D055598] (397)   Biochemical Phenomena [MESH:D001669] (328)   Molecular Structure [MESH:D015394] (174)   Base Sequence [MESH:D001483] (86)   Repetitive Sequences, Nucleic Acid [MESH:D012091] (58)   Tandem Repeat Sequences [MESH:D020080] (35)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genetic Phenomena [MESH:D055614] (1922)   Genetic Processes [MESH:D039361] (1336)   Mutagenesis [MESH:D016296] (1150)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genetic Structures [MESH:D040342] (1612)   Base Sequence [MESH:D001483] (86)   Repetitive Sequences, Nucleic Acid [MESH:D012091] (57)   Tandem Repeat Sequences [MESH:D020080] (35)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genome [MESH:D016678] (249)   Genome Components [MESH:D040481] (231)   DNA Sequence, Unstable [MESH:D043243] (28)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Tandem Repeat Sequences [MESH:D020080] (34)   DNA Repeat Expansion [MESH:D042622] (25)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  Genetic Variation [MESH:D014644] (1337)   Mutation [MESH:D009154] (1327)   DNA Repeat Expansion [MESH:D042622] (26)   Spinocerebellar Ataxia 10 [MESH:C566874] (24)  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)   Cohen syndrome [MESH:C536438] (21)