Item 7 of 17 (back to results) previous next   PCI 5002 C568608               MeSH Unique Identifier: C568608 Scope Notes: A radiation-sensitizing agent Chemical – Gene Interaction Note 1: [PCI 5002 co-treated with Zinc] results in increased expression of MARCH6 mRNA Note 2: [PCI 5002 co-treated with Zinc] results in increased expression of ABHD2 mRNA Click here for more information

Current search: C14. Cardiovascular Diseases: Cardiovascular Diseases [MESH:D002318] > Heart Diseases [MESH:D006331] > Heart Defects, Congenital [MESH:D006330] > McKusick Kaufman syndrome [MESH:C538159] × Select any link to see items in a related category. more general categories    information about this item 1. Human Genes  1. Human Genes  Adenylate kinases [HGNC:AK] (23)   TAF9 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 32kDa [HGNC:TAF9] (10)  A-kinase anchor proteins [HGNC:AKAP] (99)   ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited) [HGNC:ARFGEF2] (8)  Aldo-keto reductases [HGNC:AKR] (282)   aldo-keto reductase family 1, member C1 [HGNC:AKR1C1] (148)  Ankyrin repeat domain containing [HGNC:ANKRD] (566)   ankyrin repeat domain 11 [HGNC:ANKRD11] (18)  nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, epsilon [HGNC:NFKBIE] (19)  Argonaute/PIWI family [HGNC:AGO] (23)   argonaute RISC catalytic component 2 [HGNC:AGO2] (23)  Basic helix-loop-helix [HGNC:BHLH] (618)   inhibitor of DNA binding 2, dominant negative helix-loop-helix protein [HGNC:ID2] (69)  inhibitor of DNA binding 4, dominant negative helix-loop-helix protein [HGNC:ID4] (17)  MAX dimerization protein 1 [HGNC:MXD1] (46)  MNT, MAX dimerization protein [HGNC:MNT] (15)  Basic leucine zipper proteins [HGNC:bZIP] (670)   cAMP responsive element binding protein 1 [HGNC:CREB1] (108)  cAMP responsive element modulator [HGNC:CREM] (36)  FBJ murine osteosarcoma viral oncogene homolog [HGNC:FOS] (277)  FBJ murine osteosarcoma viral oncogene homolog B [HGNC:FOSB] (45)  jun B proto-oncogene [HGNC:JUNB] (59)  jun D proto-oncogene [HGNC:JUND] (61)  jun proto-oncogene [HGNC:JUN] (290)  Beta 3-glycosyltransferases [HGNC:B3GT] (48)   UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 [HGNC:B3GNT2] (14)  Blood group antigens [HGNC:blood-group] (97)   CD0055 molecule, decay accelerating factor for complement (Cromer blood group) [HGNC:CD55] (38)  glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) [HGNC:GCNT2] (18)  CD molecules [HGNC:CD] (1459)   CD055 molecule, decay accelerating factor for complement (Cromer blood group) [HGNC:CD55] (38)  chemokine (C-X-C motif) receptor 04 [HGNC:CXCR4] (92)  interleukin 06 receptor [HGNC:IL6R] (55)  plasminogen activator, urokinase receptor [HGNC:PLAUR] (52)  tumor necrosis factor receptor superfamily, member 10a [HGNC:TNFRSF10A] (70)  tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124)  tumor necrosis factor receptor superfamily, member 12A [HGNC:TNFRSF12A] (39)  Chemokine ligands [HGNC:CCL] (472)   chemokine (C-C motif) ligand 20 [HGNC:CCL20] (56)  chemokine (C-C motif) ligand 26 [HGNC:CCL26] (13)  Chemokine receptors [HGNC:CR] (207)   Chemokine (C-X-C motif) receptors [HGNC:CXCR] (135)   chemokine (C-X-C motif) receptor 04 [HGNC:CXCR4] (92)  Cytochrome P450s [HGNC:CYP] (1673)   cytochrome P450, family 03, subfamily A, polypeptide 05 [HGNC:CYP3A5] (134)  EF-hand domain containing [HGNC:EFHAND] (226)   protein phosphatase 3, regulatory subunit B, alpha [HGNC:PPP3R1] (10)  Endogenous Ligands [HGNC:ENDOLIG] (1191)   chemokine (C-C motif) ligand 20 [HGNC:CCL20] (56)  chemokine (C-C motif) ligand 26 [HGNC:CCL26] (13)  endothelin 1 [HGNC:EDN1] (119)  interleukin 08 [HGNC:IL8] (649)  EPH receptors [HGNC:EPH] (55)   EPH receptor A2 [HGNC:EPHA2] (24)  Ephrins [HGNC:EFN] (55)   ephrin-B2 [HGNC:EFNB2] (32)  Exostosin glycosyltransferase family [HGNC:EXT] (22)   exostosin glycosyltransferase 1 [HGNC:EXT1] (18)  Fibronectin type III domain containing [HGNC:FN3] (399)   EPH receptor A2 [HGNC:EPHA2] (24)  F-boxes [HGNC:FBX] (66)   F-boxes and WD-40 domains [HGNC:FBXW] (15)   F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase [HGNC:FBXW7] (15)  Fermitins [HGNC:FERMT] (27)   fermitin family member 2 [HGNC:FERMT2] (16)  Forkhead boxes [HGNC:FOX] (139)   forkhead box A1 [HGNC:FOXA1] (30)  GATA zinc finger domain containing [HGNC:GATAD] (101)   GATA binding protein 6 [HGNC:GATA6] (38)  General transcription factors [HGNC:GTF] (40)   general transcription factor IIH, polypeptide 1, 62kDa [HGNC:GTF2H1] (16)  General transcription factor IIH complex subunits [HGNC:TFIIH] (46)   general transcription factor IIH, polypeptide 1, 62kDa [HGNC:GTF2H1] (16)  Glycosyltransferase family 2 domain containing [HGNC:GLT2] (57)   UDP-glucose ceramide glucosyltransferase [HGNC:UGCG] (46)  Heat shock proteins [HGNC:HSP] (390)   Heat shock proteins, HSP70 [HGNC:HSP70] (294)   heat shock 105kDa/110kDa protein 01 [HGNC:HSPH1] (45)  heat shock 70kDa protein 01A [HGNC:HSPA1A] (112)  heat shock 70kDa protein 01B [HGNC:HSPA1B] (65)  heat shock 70kDa protein 01-like [HGNC:HSPA1L] (36)  heat shock 70kDa protein 04 [HGNC:HSPA4] (49)  heat shock 70kDa protein 05 (glucose-regulated protein, 78kDa) [HGNC:HSPA5] (148)  Heat shock proteins, DNAJ (HSP40) [HGNC:DNAJ] (88)   DnaJ (Hsp40) homolog, subfamily A, member 01 [HGNC:DNAJA1] (38)  DnaJ (Hsp40) homolog, subfamily B, member 06 [HGNC:DNAJB6] (23)  Heat shock proteins, HSPB (small) [HGNC:HSPB] (127)   heat shock 22kDa protein 08 [HGNC:HSPB8] (28)  heat shock 27kDa protein 01 [HGNC:HSPB1] (84)  Heat shock proteins, HSPC (HSP90) [HGNC:HSP90] (119)   heat shock protein 90kDa alpha (cytosolic), class A member 1 [HGNC:HSP90AA1] (60)  Heat shock proteins, Chaperons [HGNC:CHAP] (114)   heat shock 60kDa protein 01 (chaperonin) [HGNC:HSPD1] (66)  McKusick-Kaufman syndrome [HGNC:MKKS] (5)  t-complex 1 [HGNC:TCP1] (13)  High mobility group [HGNC:HMG] (101)   High mobility group, Non-canonical [HGNC:HMGX] (5)   high mobility group 20A [HGNC:HMG20A] (5)  Histamine receptors [HGNC:HRH] (86)   histamine receptor H1 [HGNC:HRH1] (44)  Histones [HGNC:HIST] (173)   Histones, Replication-independent [HGNC:RIH] (148)   H3 histone, family 3B (H3.3B) [HGNC:H3F3B] (13)  Histones, Replication-dependent [HGNC:HIST] (59)   histone cluster 1, H3b [HGNC:HIST1H3B] (14)  Homeoboxes [HGNC:homeobox] (219)   Homeoboxes, ANTP class [HGNC:HOXL] (152)   NKL subclass homeoboxes [HGNC:NKL] (109)   distal-less homeobox 2 [HGNC:DLX2] (23)  msh homeobox 1 [HGNC:MSX1] (19)  NK3 homeobox 1 [HGNC:NKX3-1] (42)  Homeoboxes, POU class [HGNC:POU] (49)   POU class 2 homeobox 2 [HGNC:POU2F2] (9)  Homeoboxes, TALE class [HGNC:TALE] (72)   TGFB-induced factor homeobox 1 [HGNC:TGIF1] (37)  Immunoglobulin superfamily domain containing [HGNC:IGSF] (761)   Immunoglobulin-like domain containing [HGNC:IGD] (645)   interleukin 06 receptor [HGNC:IL6R] (55)  Interleukins and interleukin receptors [HGNC:IL] (1294)   interleukin 06 receptor [HGNC:IL6R] (55)  interleukin 08 [HGNC:IL8] (649)  interleukin 11 [HGNC:IL11] (44)  K-demethylases [HGNC:KDM] (47)   lysine (K)-specific demethylase 4C [HGNC:KDM4C] (8)  Kruppel-like transcription factors [HGNC:KLF] (106)   Kruppel-like factor 02 (lung) [HGNC:KLF2] (28)  Kruppel-like factor 04 (gut) [HGNC:KLF4] (49)  Kruppel-like factor 06 [HGNC:KLF6] (56)  Kruppel-like factor 11 [HGNC:KLF11] (18)  MAX dimerization proteins [HGNC:MXD] (65)   MAX dimerization protein 1 [HGNC:MXD1] (46)  MNT, MAX dimerization protein [HGNC:MNT] (15)  Metallothioneins [HGNC:MT] (183)   metallothionein 1G [HGNC:MT1G] (56)  metallothionein 2A [HGNC:MT2A] (133)  Mitochondrial ribosomal proteins [HGNC:MRP] (52)   Mitochondrial ribosomal proteins, large subunits [HGNC:MRPL] (52)   mitochondrial ribosomal protein S06 [HGNC:MRPS6] (22)  Myocyte enhancer factors [HGNC:MEF2] (41)   myocyte enhancer factor 2A [HGNC:MEF2A] (19)  myocyte enhancer factor 2D [HGNC:MEF2D] (11)  Nuclear hormone receptors [HGNC:NR] (1322)   nuclear receptor subfamily 4, group A, member 1 [HGNC:NR4A1] (68)  nuclear receptor subfamily 4, group A, member 2 [HGNC:NR4A2] (48)  nuclear receptor subfamily 4, group A, member 3 [HGNC:NR4A3] (35)  peroxisome proliferator-activated receptor delta [HGNC:PPARD] (67)  peroxisome proliferator-activated receptor gamma [HGNC:PPARG] (234)  retinoic acid receptor, alpha [HGNC:RARA] (73)  PHD-type zinc fingers [HGNC:PHF] (103)   inhibitor of growth family, member 1 [HGNC:ING1] (9)  Phosphodiesterases [HGNC:PDE] (105)   phosphodiesterase 4D, cAMP-specific [HGNC:PDE4D] (25)  Pleckstrin homology (PH) domain containing [HGNC:PLEKH] (227)   fermitin family member 2 [HGNC:FERMT2] (16)  pleckstrin homology-like domain, family A, member 2 [HGNC:PHLDA2] (42)  protein kinase D2 [HGNC:PRKD2] (9)  son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27)  Poly (ADP-ribose) polymerases [HGNC:PARP] (56)   TCDD-inducible poly(ADP-ribose) polymerase [HGNC:TIPARP] (42)  Protein phosphatase, catalytic and regulatory subunits [HGNC:PPP-PPM-CTD] (225)   Protein phosphatase 3, regulatory subunits [HGNC:PPP3R] (10)   protein phosphatase 3, regulatory subunit B, alpha [HGNC:PPP3R1] (10)  Protein phosphatases, Mg2+/Mn2+ dependent [HGNC:PPM] (58)   protein phosphatase, Mg2+/Mn2+ dependent, 1D [HGNC:PPM1D] (34)  Protein tyrosine phosphatases, including dual specificity phosphatases [HGNC:PTP] (254)   Protein tyrosine phosphatases, Class I Cys-based [HGNC:PTPN] (252)   Class I Cys-based PTPs : Non-receptor [HGNC:PTPN] (75)   protein tyrosine phosphatase, non-receptor type 22 (lymphoid) [HGNC:PTPN22] (11)  Class I Cys-based PTPs : MAP kinase phosphatases [HGNC:DUSPT] (127)   dual specificity phosphatase 01 [HGNC:DUSP1] (91)  dual specificity phosphatase 10 [HGNC:DUSP10] (34)  RAB, member RAS oncogene [HGNC:RAB] (69)   RAB07A, member RAS oncogene family [HGNC:RAB7A] (7)  Regulators of G-protein signaling [HGNC:RGS] (98)   regulator of G-protein signaling 02, 24kDa [HGNC:RGS2] (44)  Rho guanine nucleotide exchange factors [HGNC:ARHGEF] (105)   son of sevenless homolog 1 (Drosophila) [HGNC:SOS1] (27)  RNA binding motif containing [HGNC:RRM] (251)   serine/arginine-rich splicing factor 05 [HGNC:SRSF5] (22)  RING-type zinc fingers [HGNC:RNF] (151)   BRCA1 associated protein [HGNC:BRAP] (4)  CCHC-type zinc finger, nucleic acid binding protein [HGNC:CNBP] (16)  ring finger and WD repeat domain 3 [HGNC:RFWD3] (11)  ZFP36 ring finger protein [HGNC:ZFP36] (44)  Serine/arginine-rich splicing factors [HGNC:SRSF] (62)   serine/arginine-rich splicing factor 05 [HGNC:SRSF5] (22)  Serine (or cysteine) peptidase inhibitors [HGNC:SERPIN] (252)   serpin peptidase inhibitor, clade B (ovalbumin), member 08 [HGNC:SERPINB8] (23)  serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 [HGNC:SERPINE1] (138)  SH2 domain containing [HGNC:SH2D] (431)   suppressor of cytokine signaling 2 [HGNC:SOCS2] (31)  suppressor of cytokine signaling 3 [HGNC:SOCS3] (46)  SKI transcriptional corepressors [HGNC:SKOR] (22)   SKI-like oncogene [HGNC:SKIL] (15)  Snail homologs [HGNC:SNAI] (56)   snail family zinc finger 1 [HGNC:SNAI1] (41)  snail family zinc finger 2 [HGNC:SNAI2] (28)  Solute carriers [HGNC:SLC] (716)   solute carrier family 02 (facilitated glucose transporter), member 03 [HGNC:SLC2A3] (76)  solute carrier family 07 (anionic amino acid transporter light chain, xc- system), member 11 [HGNC:SLC7A11] (77)  solute carrier family 20 (phosphate transporter), member 01 [HGNC:SLC20A1] (30)  solute carrier family 23 (ascorbic acid transporter), member 2 [HGNC:SLC23A2] (22)  solute carrier family 26 (anion exchanger), member 2 [HGNC:SLC26A2] (24)  solute carrier family 30 (zinc transporter), member 1 [HGNC:SLC30A1] (46)  solute carrier family 33 (acetyl-CoA transporter), member 1 [HGNC:SLC33A1] (13)  solute carrier family 39 (zinc transporter), member 10 [HGNC:SLC39A10] (20)  uncoupling protein 3 (mitochondrial, proton carrier) [HGNC:UCP3] (11)  SRY (sex determining region Y)-boxes [HGNC:SOX] (95)   SRY (sex determining region Y)-box 08 [HGNC:SOX8] (7)  Sterile alpha motif (SAM) containing [HGNC:SAMD] (92)   EPH receptor A2 [HGNC:EPHA2] (24)  sterile alpha motif domain containing 4A [HGNC:SAMD4A] (17)  Suppressors of cytokine signaling [HGNC:SOCS] (82)   suppressor of cytokine signaling 2 [HGNC:SOCS2] (31)  suppressor of cytokine signaling 3 [HGNC:SOCS3] (46)  Syndecans (transmembrane HSPG) [HGNC:SDC] (36)   syndecan 4 [HGNC:SDC4] (29)  T-boxes [HGNC:TBX] (49)   T-box 03 [HGNC:TBX3] (24)  Tetratricopeptide repeat domain containing [HGNC:TTC] (153)   SH3 domain and tetratricopeptide repeats 1 [HGNC:SH3TC1] (6)  Tubulins [HGNC:TUB] (87)   tubulin, beta 3 class III [HGNC:TUBB3] (33)  Tudor domain containing [HGNC:TDRD] (64)   lysine (K)-specific demethylase 4C [HGNC:KDM4C] (8)  Tumor necrosis factor (ligand) superfamily [HGNC:TNFSF] (898)   tumor necrosis factor (ligand) superfamily, member 09 [HGNC:TNFSF9] (37)  Tumor necrosis factor receptor superfamily [HGNC:TNFRSF] (295)   tumor necrosis factor receptor superfamily, member 10a [HGNC:TNFRSF10A] (70)  tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124)  tumor necrosis factor receptor superfamily, member 12A [HGNC:TNFRSF12A] (39)  Ubiquitin-conjugating enzymes E2 [HGNC:UBE2] (97)   ubiquitin-conjugating enzyme E2H [HGNC:UBE2H] (17)  WD repeat domain containing [HGNC:WDR] (199)   F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase [HGNC:FBXW7] (15)  platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa) [HGNC:PAFAH1B1] (18)  ring finger and WD repeat domain 3 [HGNC:RFWD3] (11)  ZINC FINGERS [HGNC:ZNF] (383)   Zinc fingers, C2H2-type [HGNC:ZNF] (349)   early growth response 1 [HGNC:EGR1] (140)  early growth response 2 [HGNC:EGR2] (37)  Kruppel-like factor 02 (lung) [HGNC:KLF2] (28)  Kruppel-like factor 04 (gut) [HGNC:KLF4] (49)  Kruppel-like factor 06 [HGNC:KLF6] (56)  Kruppel-like factor 11 [HGNC:KLF11] (18)  snail family zinc finger 1 [HGNC:SNAI1] (41)  snail family zinc finger 2 [HGNC:SNAI2] (28)  Zinc fingers, C2H2-type with KRAB domain [HGNC:ZKRAB] (42)   zinc finger protein 331 [HGNC:ZNF331] (8)  Zinc fingers, C2H2-type with BTB/POZ domain [HGNC:ZBTB] (35)   zinc finger and BTB domain containing 20 [HGNC:ZBTB20] (17)  Other zinc fingers [HGNC:] (148)   Zinc fingers, C2CH-type [HGNC:THAP domain containing] (5)   THAP domain containing, apoptosis associated protein 1 [HGNC:THAP1] (5)  Zinc fingers, CCCH-type [HGNC:ZC3H] (17)   zinc finger CCCH-type containing 12A [HGNC:ZC3H12A] (12)  Zinc fingers, CCHC-type [HGNC:ZCCHC ] (40)   CCHC-type zinc finger, nucleic acid binding protein [HGNC:CNBP] (16) 2. Interaction: Human Genes and Chemicals  2. Interaction: Human Genes and Chemicals  Affects (3990)   cotreatment (1499)  Decreases (5154)   expression (2187)  Increases (5571)   expression (3238) A. Anatomy  A. Anatomy  Body Regions [MESH:D001829] (867)   Head [MESH:D006257] (523)   Face [MESH:D005145] (387)   Coffin-Siris syndrome [MESH:C536436] (102)  Neck [MESH:D009333] (107)   Coffin-Siris syndrome [MESH:C536436] (102)  Musculoskeletal System [MESH:D009141] (1255)   Skeleton [MESH:D012863] (1177)   Bone and Bones [MESH:D001842] (1112)   Bones of Lower Extremity [MESH:D050281] (278)   Leg Bones [MESH:D007867] (228)   Patella [MESH:D010329] (168)   Epiphyseal dysplasia, multiple, 4 [MESH:C535504] (34)  Bones of Upper Extremity [MESH:D001133] (240)   Arm Bones [MESH:D050280] (183)   Ulna [MESH:D014457] (96)   Ulnar-mammary syndrome [MESH:C536937] (57)  Epiphyses [MESH:D004838] (98)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Valves [MESH:D006351] (666)   Aortic Valve [MESH:D001021] (659)   Aortic Valve, Calcification of [MESH:C562942] (655)  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, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Toxemia [MESH:D014115] (1290)   Endotoxemia [MESH:D019446] (1289) C02. Virus Diseases  C02. Virus Diseases  Virus Diseases [MESH:D014777] (4544)   DNA Virus Infections [MESH:D004266] (2474)   Herpesviridae Infections [MESH:D006566] (1944)   Epstein-Barr Virus Infections [MESH:D020031] (695)   Burkitt Lymphoma [MESH:D002051] (691)  Papillomavirus Infections [MESH:D030361] (630)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  RNA Virus Infections [MESH:D012327] (4215)   Orthomyxoviridae Infections [MESH:D009976] (1077)   Influenza, Human [MESH:D007251] (1075)  Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Tumor Virus Infections [MESH:D014412] (1069)   Papillomavirus Infections [MESH:D030361] (537)  Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Protozoan Infections [MESH:D011528] (3014)   Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Parasitic [MESH:D012876] (2541)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Hamartoma [MESH:D006222] (1484)  Neoplasms, Second Primary [MESH:D016609] (518)  Precancerous Conditions [MESH:D011230] (2858)  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)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphatic Vessel Tumors [MESH:D018190] (171)   Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Rhabdoid Tumor [MESH:D018335] (61)   Rhabdoid Tumor Predisposition Syndrome 2 [MESH:C567643] (43)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Neoplasms, Adipose Tissue [MESH:D018205] (677)   Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Neoplasms, Connective Tissue [MESH:D009372] (3626)   Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Mastocytosis [MESH:D008415] (792)   Mastocytosis, Systemic [MESH:D034721] (769)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)  Neoplasms, Fibrous Tissue [MESH:D018218] (1720)   Solitary Fibrous Tumors [MESH:D054364] (79)  Histiocytoma [MESH:D051642] (272)   Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Smooth Muscle Tumor [MESH:D018235] (132)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Perivascular Epithelioid Cell Neoplasms [MESH:D054973] (165)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Sarcoma [MESH:D012509] (4246)   Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)  Histiocytoma, Malignant Fibrous [MESH:D051677] (266)   Histiocytoma, Angiomatoid Fibrous [MESH:C563181] (258)  Liposarcoma [MESH:D008080] (612)   Liposarcoma, Myxoid [MESH:D018208] (358)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Mesothelioma [MESH:D008654] (2567)  Adenoma, Oxyphilic [MESH:D018249] (115)   Oncocytoma, renal [MESH:C537750] (35)  Carcinoma [MESH:D002277] (7263)   Carcinoma, Transitional Cell [MESH:D002295] (2662)  Adenocarcinoma [MESH:D000230] (6565)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Adenoid Cystic [MESH:D003528] (1561)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Adenocarcinoma, Follicular [MESH:D018263] (677)   Thyroid cancer, follicular [MESH:C572845] (674)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  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, Ductal, Breast [MESH:D018270] (1112)  Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Papilloma [MESH:D010212] (2243)  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)   Meningioma, familial [MESH:C537443] (195)  Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Gliosarcoma [MESH:D018316] (880)  Medulloblastoma [MESH:D008527] (1282)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  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)  Hemangioma [MESH:D006391] (690)   Hemangioma, Capillary [MESH:D018324] (503)   Hemangioblastoma [MESH:D018325] (395)  Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  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)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Digestive System Neoplasms [MESH:D004067] (7487)   Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Head and Neck Neoplasms [MESH:D006258] (4612)   Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)  Thyroid Neoplasms [MESH:D013964] (2040)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Tongue Neoplasms [MESH:D014062] (1518)  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)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Skin Neoplasms [MESH:D012878] (2992)   Familial cylindromatosis [MESH:C536611] (35)  Thoracic Neoplasms [MESH:D013899] (6032)   Respiratory Tract Neoplasms [MESH:D012142] (6020)   Lung Neoplasms [MESH:D008175] (6015)   Adenocarcinoma of lung [MESH:C538231] (1487)  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, Female [MESH:D005833] (2540)   Uterine Neoplasms [MESH:D014594] (2431)   Endometrial Neoplasms [MESH:D016889] (1987)  Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Oncocytoma, renal [MESH:C537750] (35)  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 Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Familial cylindromatosis [MESH:C536611] (35)  Meningioma, familial [MESH:C537443] (195)  Birt-Hogg-Dube Syndrome [MESH:D058249] (35)  Exostoses, Multiple Hereditary [MESH:D005097] (154)  Tumor Virus Infections [MESH:D014412] (759)   Epstein-Barr Virus Infections [MESH:D020031] (693)   Burkitt Lymphoma [MESH:D002051] (691)  Warts [MESH:D014860] (167)   WHIM syndrome [MESH:C536697] (148) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Cartilage Diseases [MESH:D002357] (438)  Bone Diseases [MESH:D001847] (5801)   Bone Neoplasms [MESH:D001859] (1334)  Osteitis Deformans [MESH:D010001] (287)  Bone Diseases, Developmental [MESH:D001848] (3315)   Dwarfism [MESH:D004392] (778)   Desbuquois syndrome [MESH:C535943] (20)  Diastrophic dysplasia [MESH:C536170] (34)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1B [MESH:C536016] (34)  Osteochondrodysplasias [MESH:D010009] (2440)   Atelosteogenesis type 2 [MESH:C535395] (34)  Epiphyseal dysplasia, multiple, 4 [MESH:C535504] (34)  Wolcott-Rallison syndrome [MESH:C536739] (92)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Fibrous Dysplasia of Bone [MESH:D005357] (737)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1B [MESH:C536016] (34)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)  Osteosclerosis [MESH:D010026] (356)   Osteopetrosis [MESH:D010022] (318)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)  Hyperostosis [MESH:D015576] (493)   Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)  Spinal Diseases [MESH:D013122] (2485)   Spinal Curvatures [MESH:D013121] (742)   Kyphosis [MESH:D007738] (637)  Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Joint Diseases [MESH:D007592] (4657)   Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Joint Instability [MESH:D007593] (67)   Desbuquois syndrome [MESH:C535943] (20)  Muscular Diseases [MESH:D009135] (4071)   Muscle Rigidity [MESH:D009127] (617)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myotonic Disorders [MESH:D020967] (138)   Dystrophia myotonica 2 [MESH:C538009] (34)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Desbuquois syndrome [MESH:C535943] (20)  Costello Syndrome [MESH:D056685] (407)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Limb Deformities, Congenital [MESH:D017880] (1813)   Polydactyly [MESH:D017689] (318)   Desbuquois syndrome [MESH:C535943] (20)  McKusick Kaufman syndrome [MESH:C538159] (17)  Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  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)  Digestive System Abnormalities [MESH:D004065] (2127)   Barrett Esophagus [MESH:D001471] (1930)  Digestive System Neoplasms [MESH:D004067] (7493)   Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Gastrointestinal Diseases [MESH:D005767] (7443)   Esophageal Diseases [MESH:D004935] (4255)   Barrett Esophagus [MESH:D001471] (1930)  Deglutition Disorders [MESH:D003680] (1538)   Esophageal Motility Disorders [MESH:D015154] (1489)   Gastroesophageal Reflux [MESH:D005764] (1465)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Esophagitis [MESH:D004941] (1120)   Eosinophilic Esophagitis [MESH:D057765] (43)  Esophagitis, Peptic [MESH:D004942] (709)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Esophagitis [MESH:D004941] (1120)   Eosinophilic Esophagitis [MESH:D057765] (43)  Esophagitis, Peptic [MESH:D004942] (709)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Crohn Disease [MESH:D003424] (2585)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  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)  Enterocolitis [MESH:D004760] (1536)   Enterocolitis, Necrotizing [MESH:D020345] (1367)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   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)  Malabsorption Syndromes [MESH:D008286] (492)   Celiac Disease [MESH:D002446] (340)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Peptic Ulcer [MESH:D010437] (3172)   Esophagitis, Peptic [MESH:D004942] (709)  Stomach Ulcer [MESH:D013276] (2915)  Stomach Diseases [MESH:D013272] (5325)   Gastroparesis [MESH:D018589] (732)  Stomach Neoplasms [MESH:D013274] (4942)  Peptic Ulcer [MESH:D010437] (2994)   Stomach Ulcer [MESH:D013276] (2915)  Liver Diseases [MESH:D008107] (8167)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Cholestasis, Intrahepatic [MESH:D002780] (1510)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Hepatitis [MESH:D006505] (3883)  Hepatomegaly [MESH:D006529] (1169)  Hepatorenal Syndrome [MESH:D006530] (910)  Hypertension, Portal [MESH:D006975] (869)  Fatty Liver [MESH:D005234] (3584)   Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  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)   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)   Orofacial Cleft 5 [MESH:C563843] (38)  PCI 5002 [MESH:C568608] (527)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Oral Submucous Fibrosis [MESH:D009914] (2432)  Oral Ulcer [MESH:D019226] (488)  Lip Diseases [MESH:D008047] (924)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  PCI 5002 [MESH:C568608] (433)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  PCI 5002 [MESH:C568608] (433)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Mouth Neoplasms [MESH:D009062] (2263)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Periodontal Diseases [MESH:D010510] (1001)   Periapical Diseases [MESH:D010483] (186)   Periapical Periodontitis [MESH:D010485] (183)  Periodontitis [MESH:D010518] (843)   Periapical Periodontitis [MESH:D010485] (183)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)   Orstavik Lindemann Solberg syndrome [MESH:C537137] (668)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  Orofacial Cleft 12 [MESH:C567548] (434)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535)  Tooth Abnormalities [MESH:D014071] (622)   Tooth Agenesis, Selective, 6 [MESH:C567755] (154)  Anodontia [MESH:D000848] (185)   Witkop syndrome [MESH:C536736] (38)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Hypomaturation Type, Iia3 [MESH:C567706] (22)  Tooth Diseases [MESH:D014076] (742)   Tooth Abnormalities [MESH:D014071] (622)   Tooth Agenesis, Selective, 6 [MESH:C567755] (154)  Anodontia [MESH:D000848] (185)   Witkop syndrome [MESH:C536736] (38)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Hypomaturation Type, Iia3 [MESH:C567706] (22) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Lung Diseases [MESH:D008171] (7249)   Hypertension, Pulmonary [MESH:D006976] (2000)  Pneumonia [MESH:D011014] (3482)  Pulmonary Embolism [MESH:D011655] (1118)  Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Idiopathic Interstitial Pneumonias [MESH:D054988] (314)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Bronchitis [MESH:D001991] (993)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Bronchitis, Chronic [MESH:D029481] (569)  Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Acute Lung Injury [MESH:D055371] (1907)  Lung Neoplasms [MESH:D008175] (6012)   Adenocarcinoma of lung [MESH:C538231] (1487)  Carcinoma, Bronchogenic [MESH:D002283] (3606)   Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)  Small Cell Lung Carcinoma [MESH:D055752] (1380)  Pulmonary Fibrosis [MESH:D011658] (3140)   Idiopathic Pulmonary Fibrosis [MESH:D054990] (310)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134)  Pleural Diseases [MESH:D010995] (2240)   Pneumothorax [MESH:D011030] (42)   Pneumothorax, Primary Spontaneous [MESH:C566795] (35)  Respiration Disorders [MESH:D012120] (2218)   Respiratory Distress Syndrome, Adult [MESH:D012128] (864)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Influenza, Human [MESH:D007251] (1075)  Pneumonia [MESH:D011014] (3482)  Rhinitis [MESH:D012220] (766)  Bronchitis [MESH:D001991] (588)   Bronchitis, Chronic [MESH:D029481] (569)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   Adenocarcinoma of lung [MESH:C538231] (1487)  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)  Nose Diseases [MESH:D009668] (1504)   Rhinitis [MESH:D012220] (1134) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Chronobiology Disorders [MESH:D021081] (970)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Edema [MESH:D001929] (1165)  Brain Injuries [MESH:D001930] (3429)  Brain Neoplasms [MESH:D001932] (2764)  Basal Ganglia Diseases [MESH:D001480] (4268)   Huntington Disease [MESH:D006816] (540)  Supranuclear Palsy, Progressive [MESH:D013494] (235)  Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Pantothenate Kinase-Associated Neurodegeneration [MESH:D006211] (17)   Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration [MESH:C564603] (16)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Cerebellar Diseases [MESH:D002526] (736)   Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 1 [MESH:C537308] (21)  Cerebrovascular Disorders [MESH:D002561] (5542)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  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)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  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)  Huntington Disease [MESH:D006816] (540)  Lewy Body Disease [MESH:D020961] (1143)  Epilepsy [MESH:D004827] (6274)   Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Partial [MESH:D004828] (1267)   Epilepsy, Temporal Lobe [MESH:D004833] (1108)  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)   Migraine without Aura [MESH:D020326] (408)  Hypothalamic Diseases [MESH:D007027] (1833)   Bardet-Biedl Syndrome [MESH:D020788] (110)  Pituitary Diseases [MESH:D010900] (1808)   Hyperpituitarism [MESH:D006964] (1250)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Leukoencephalopathies [MESH:D056784] (1916)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (822)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Neuroaxonal Dystrophies [MESH:D019150] (100)   Neurodegeneration with brain iron accumulation (NBIA) [MESH:C538421] (30)  Pantothenate Kinase-Associated Neurodegeneration [MESH:D006211] (17)   Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration [MESH:C564603] (16)  Movement Disorders [MESH:D009069] (4823)   Supranuclear Palsy, Progressive [MESH:D013494] (235)  Dyskinesias [MESH:D020820] (1827)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)  Dystonic Disorders [MESH:D020821] (729)   Dystonia, Dopa-responsive [MESH:C538007] (98)  Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Pantothenate Kinase-Associated Neurodegeneration [MESH:D006211] (17)   Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration [MESH:C564603] (16)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Parkinson Disease, Secondary [MESH:D010302] (327)  Ocular Motility Disorders [MESH:D015835] (364)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Spinal Cord Diseases [MESH:D013118] (4376)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 4, Juvenile [MESH:C566550] (21)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 1 [MESH:C537308] (21)  Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)  Optic Nerve Diseases [MESH:D009901] (1375)   Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Demyelinating Diseases [MESH:D003711] (2917)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (2035)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Absent corpus callosum cataract immunodeficiency [MESH:C535566] (11)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Hereditary Motor And Sensory Neuropathy VI [MESH:C562851] (31)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth disease, Type 2B [MESH:C537989] (15)  Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (31)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 6, autosomal dominant [MESH:C536866] (12)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Spastic Paraplegia 42, Autosomal Dominant [MESH:C567262] (22)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Periventricular Nodular Heterotopia [MESH:D054091] (51)   Heterotopia, Periventricular, Autosomal Recessive [MESH:C564292] (14)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)  Meningeal Neoplasms [MESH:D008577] (984)   Meningioma [MESH:D008579] (978)   Meningioma, familial [MESH:C537443] (195)  Neurodegenerative Diseases [MESH:D019636] (6613)   Lewy Body Disease [MESH:D020961] (1143)  Parkinson Disease [MESH:D010300] (3595)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Huntington Disease [MESH:D006816] (540)  Rett Syndrome [MESH:D015518] (143)  Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Hereditary Motor And Sensory Neuropathy VI [MESH:C562851] (31)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth disease, Type 2B [MESH:C537989] (15)  Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (31)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 6, autosomal dominant [MESH:C536866] (12)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Spastic Paraplegia 42, Autosomal Dominant [MESH:C567262] (22)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Pantothenate Kinase-Associated Neurodegeneration [MESH:D006211] (17)   Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration [MESH:C564603] (16)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 1 [MESH:C537308] (21)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 4, Juvenile [MESH:C566550] (21)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)  Supranuclear Palsy, Progressive [MESH:D013494] (235)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 4, Juvenile [MESH:C566550] (21)  Neurologic Manifestations [MESH:D009461] (8964)   Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Ataxia [MESH:D001259] (1138)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tics [MESH:D020323] (62)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Memory Disorders [MESH:D008569] (3233)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)   Articulation Disorders [MESH:D001184] (164)   Dysarthria [MESH:D004401] (163)  Intellectual Disability [MESH:D008607] (3054)   Coffin-Siris syndrome [MESH:C536436] (102)  Down Syndrome [MESH:D004314] (1287)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3875)   Pain, Intractable [MESH:D010148] (707)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)  Sensation Disorders [MESH:D012678] (5011)   Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Amyotrophic Lateral Sclerosis 4, Juvenile [MESH:C566550] (21)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Atrophy, Spinal [MESH:D009134] (377)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Muscular Diseases [MESH:D009135] (3538)   Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Myotonic Disorders [MESH:D020967] (138)   Dystrophia myotonica 2 [MESH:C538009] (34)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Mononeuropathies [MESH:D020422] (604)   Sciatic Neuropathy [MESH:D020426] (477)  Neuralgia [MESH:D009437] (2078)   Neuralgia, Postherpetic [MESH:D051474] (742)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Hereditary Motor And Sensory Neuropathy VI [MESH:C562851] (31)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth disease, Type 2B [MESH:C537989] (15)  Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (31)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 6, autosomal dominant [MESH:C536866] (12)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Spastic Paraplegia 42, Autosomal Dominant [MESH:C567262] (22)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Trauma, Nervous System [MESH:D020196] (3997)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Corneal Diseases [MESH:D003316] (1445)   Corneal Neovascularization [MESH:D016510] (622)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Albinism [MESH:D000417] (258)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)   Absent corpus callosum cataract immunodeficiency [MESH:C535566] (11)  Ocular Motility Disorders [MESH:D015835] (1699)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)  Optic Nerve Diseases [MESH:D009901] (1377)   Optic Neuritis [MESH:D009902] (273)   Neuromyelitis Optica [MESH:D009471] (248)  Orbital Diseases [MESH:D009916] (317)   Exophthalmos [MESH:D005094] (297)   Graves Disease [MESH:D006111] (278)  Retinal Diseases [MESH:D012164] (3747)   Diabetic Retinopathy [MESH:D003930] (1371)  Retinal Detachment [MESH:D012163] (1639)  Retinal Vein Occlusion [MESH:D012170] (607)  Retinal Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Edema [MESH:D008269] (557)  Uveal Diseases [MESH:D014603] (2428)   Choroid Diseases [MESH:D015862] (595)   Choroidal Neovascularization [MESH:D020256] (550)  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)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)   Asthenozoospermia [MESH:D053627] (298)  Penile Diseases [MESH:D010409] (1805)   Hypospadias [MESH:D007021] (798)   Hypospadias 2, X-Linked [MESH:C567462] (16)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Sexual Dysfunction, Physiological [MESH:D012735] (1808)   Erectile Dysfunction [MESH:D007172] (1791)  Urogenital Abnormalities [MESH:D014564] (2065)   Hypospadias [MESH:D007021] (798)   Hypospadias 2, X-Linked [MESH:C567462] (16)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Oncocytoma, renal [MESH:C537750] (35)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Oncocytoma, renal [MESH:C537750] (35)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  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)   Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Urinary Bladder Diseases [MESH:D001745] (4374)   Cystitis [MESH:D003556] (604)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)  Urinary Retention [MESH:D016055] (411) 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)  Infertility [MESH:D007246] (2211)   Infertility, Female [MESH:D007247] (2184)  Uterine Diseases [MESH:D014591] (2479)   McKusick Kaufman syndrome [MESH:C538159] (17)  Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  Vaginal Diseases [MESH:D014623] (446)   Hydrocolpos [MESH:D052202] (18)   McKusick Kaufman syndrome [MESH:C538159] (17)  Urogenital Abnormalities [MESH:D014564] (2043)   Hypospadias [MESH:D007021] (798)   Hypospadias 2, X-Linked [MESH:C567462] (16)  Hypospadias 1, X-Linked [MESH:C567482] (571)  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)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Oncocytoma, renal [MESH:C537750] (35)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Anuria [MESH:D001002] (833)  Diabetic Nephropathies [MESH:D003928] (2301)  Hepatorenal Syndrome [MESH:D006530] (910)  Kidney Diseases, Cystic [MESH:D052177] (1009)   Polycystic Kidney Diseases [MESH:D007690] (853)   Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522)  Kidney Neoplasms [MESH:D007680] (3966)   Oncocytoma, renal [MESH:C537750] (35)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, IGA [MESH:D005922] (897)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  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)   Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Urinary Bladder Diseases [MESH:D001745] (4375)   Cystitis [MESH:D003556] (604)  Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urinary Bladder, Overactive [MESH:D053201] (530)  Urination Disorders [MESH:D014555] (3598)   Anuria [MESH:D001002] (833)  Hematuria [MESH:D006417] (477)  Proteinuria [MESH:D011507] (3293)  Urinary Retention [MESH:D016055] (411)  Pregnancy Complications [MESH:D011248] (4768)   Abortion, Spontaneous [MESH:D000022] (2780)  Diabetes, Gestational [MESH:D016640] (1157)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435)  Obstetric Labor Complications [MESH:D007744] (1550)   Fetal Membranes, Premature Rupture [MESH:D005322] (356)  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)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  McKusick Kaufman syndrome [MESH:C538159] (17)  Heart Septal Defects [MESH:D006343] (385)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Transposition of Great Vessels [MESH:D014188] (60)   Transposition of the Great Arteries, Dextro-Looped 1 [MESH:C563853] (28)  Heart Diseases [MESH:D006331] (8614)   Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  McKusick Kaufman syndrome [MESH:C538159] (17)  Heart Septal Defects [MESH:D006343] (385)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Transposition of Great Vessels [MESH:D014188] (60)   Transposition of the Great Arteries, Dextro-Looped 1 [MESH:C563853] (28)  Heart Rupture [MESH:D006341] (141)   Heart Rupture, Post-Infarction [MESH:D006342] (137)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Valve, Calcification of [MESH:C562942] (655)  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)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Coronary Disease [MESH:D003327] (3439)   Coronary Stenosis [MESH:D023921] (1806)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Myocardial Infarction [MESH:D009203] (4122)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Ventricular Outflow Obstruction [MESH:D014694] (976)   Aortic Valve Stenosis [MESH:D001024] (810)   Aortic Valve, Calcification of [MESH:C562942] (655)  Vascular Diseases [MESH:D014652] (8691)   Hypotension [MESH:D007022] (4045)  Retinal Vein Occlusion [MESH:D012170] (607)  Vascular System Injuries [MESH:D057772] (2086)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Cerebrovascular Disorders [MESH:D002561] (5541)   Carotid Artery Diseases [MESH:D002340] (1993)  Brain Ischemia [MESH:D002545] (4873)   Ischemic Attack, Transient [MESH:D002546] (1313)  Brain Infarction [MESH:D020520] (2571)   Cerebral Infarction [MESH:D002544] (2458)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)  Subarachnoid Hemorrhage [MESH:D013345] (1082)  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)  Embolism, Fat [MESH:D004620] (261)   Embolism, Cholesterol [MESH:D017700] (255)  Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  Thrombosis [MESH:D013927] (3101)   Thromboembolism [MESH:D013923] (732)   Intracranial Embolism and Thrombosis [MESH:D002542] (550)   Intracranial Thrombosis [MESH:D020767] (481)   Sinus Thrombosis, Intracranial [MESH:D012851] (356)   Sagittal Sinus Thrombosis [MESH:D020225] (223)  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)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Coronary Disease [MESH:D003327] (3439)   Coronary Stenosis [MESH:D023921] (1806)  Coronary Artery Disease [MESH:D003324] (2685)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Myocardial Infarction [MESH:D009203] (4151)   Coronary Artery Disease, Autosomal Dominant, 1 [MESH:C564258] (46)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Vasculitis [MESH:D014657] (2604)   Behcet Syndrome [MESH:D001528] (1784)  Purpura, Schoenlein-Henoch [MESH:D011695] (266) C15. Hemic and Lymphatic Diseases  C15. Hemic and Lymphatic Diseases  Hematologic Diseases [MESH:D006402] (6174)   Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)  Anemia, Sideroblastic [MESH:D000756] (636)  Anemia, Macrocytic [MESH:D000748] (382)   5q- syndrome [MESH:C535323] (131)  Blood Coagulation Disorders [MESH:D001778] (1828)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Coagulation Disorders, Inherited [MESH:D025861] (720)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Blood Platelet Disorders [MESH:D001791] (3174)   Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Blood Protein Disorders [MESH:D001796] (3051)   Agammaglobulinemia [MESH:D000361] (156)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic Syndromes [MESH:D009190] (2093)   Anemia, Sideroblastic [MESH:D000756] (636)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Thrombocytosis [MESH:D013922] (720)   Thrombocythemia, Essential [MESH:D013920] (707)  Hemorrhagic Disorders [MESH:D006474] (3359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)  Thrombocythemia, Essential [MESH:D013920] (707)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Platelet Storage Pool Deficiency [MESH:D010981] (84)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Leukocyte Disorders [MESH:D007960] (2662)   Leukostasis [MESH:D018921] (769)  Eosinophilia [MESH:D004802] (537)   Eosinophilic Esophagitis [MESH:D057765] (43)  Leukopenia [MESH:D007970] (1921)   Agranulocytosis [MESH:D000380] (1675)   Neutropenia [MESH:D009503] (1629)  Lymphatic Diseases [MESH:D008206] (5167)   Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Agammaglobulinemia [MESH:D000361] (156)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  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)   Coffin-Siris syndrome [MESH:C536436] (102)  Ulnar-mammary syndrome [MESH:C536937] (57)  McKusick Kaufman syndrome [MESH:C538159] (17)  Cold-Induced Sweating Syndrome 1 [MESH:C564791] (29)  Bardet-Biedl Syndrome [MESH:D020788] (110)  Costello Syndrome [MESH:D056685] (407)  Down Syndrome [MESH:D004314] (1287)  Wolf-Hirschhorn Syndrome [MESH:D054877] (72)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Waardenburg Syndrome [MESH:D014849] (243)   Waardenburg Syndrome, Type 2D [MESH:C563839] (48)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  McKusick Kaufman syndrome [MESH:C538159] (17)  Heart Septal Defects [MESH:D006343] (385)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Transposition of Great Vessels [MESH:D014188] (60)   Transposition of the Great Arteries, Dextro-Looped 1 [MESH:C563853] (28)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Wolf-Hirschhorn Syndrome [MESH:D054877] (72)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Desbuquois syndrome [MESH:C535943] (20)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Limb Deformities, Congenital [MESH:D017880] (1813)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Polydactyly [MESH:D017689] (318)   Desbuquois syndrome [MESH:C535943] (20)  McKusick Kaufman syndrome [MESH:C538159] (17)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Absent corpus callosum cataract immunodeficiency [MESH:C535566] (11)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Hereditary Motor And Sensory Neuropathy VI [MESH:C562851] (31)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth disease, Type 2B [MESH:C537989] (15)  Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (31)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 6, autosomal dominant [MESH:C536866] (12)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Spastic Paraplegia 42, Autosomal Dominant [MESH:C567262] (22)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Malformations of Cortical Development [MESH:D054220] (1406)   Lissencephaly [MESH:D054082] (218)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Neuronal Migration Disorders [MESH:D054081] (264)   Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Periventricular Nodular Heterotopia [MESH:D054091] (51)   Heterotopia, Periventricular, Autosomal Recessive [MESH:C564292] (14)  Skin Abnormalities [MESH:D012868] (1723)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Lip [MESH:D002971] (914)   Orofacial Cleft 5 [MESH:C563843] (38)  Cleft Palate [MESH:D002972] (1330)   Orofacial Cleft 5 [MESH:C563843] (38)  Tooth Abnormalities [MESH:D014071] (622)   Anodontia [MESH:D000848] (185)   Witkop syndrome [MESH:C536736] (38)  Dental Enamel Hypoplasia [MESH:D003744] (69)   Amelogenesis Imperfecta [MESH:D000567] (57)   Amelogenesis Imperfecta, Hypomaturation Type, Iia3 [MESH:C567706] (12)  Urogenital Abnormalities [MESH:D014564] (2064)   Hypospadias [MESH:D007021] (798)   Hypospadias 2, X-Linked [MESH:C567462] (16)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Genetic Diseases, Inborn [MESH:D030342] (9766)   Costello Syndrome [MESH:D056685] (407)  Blood Coagulation Disorders, Inherited [MESH:D025861] (722)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Chromosome Disorders [MESH:D025063] (2030)   Down Syndrome [MESH:D004314] (1287)  Wolf-Hirschhorn Syndrome [MESH:D054877] (72)  Holoprosencephaly [MESH:D016142] (218)   Holoprosencephaly 4 [MESH:C564180] (70)  Dwarfism [MESH:D004392] (783)   Desbuquois syndrome [MESH:C535943] (20)  Diastrophic dysplasia [MESH:C536170] (34)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Achondroplasia [MESH:D000130] (196)   Achondrogenesis type 1B [MESH:C536016] (34)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Hypospadias 2, X-Linked [MESH:C567462] (16)  Hypospadias 1, X-Linked [MESH:C567482] (571)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Adrenoleukodystrophy [MESH:D000326] (1348)  Classical Lissencephalies and Subcortical Band Heterotopias [MESH:D054221] (114)  Rett Syndrome [MESH:D015518] (143)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Huntington Disease [MESH:D006816] (540)  Rett Syndrome [MESH:D015518] (143)  Dystonia Musculorum Deformans [MESH:D004422] (38)   Dystonia 6, torsion [MESH:C538003] (13)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Hereditary Motor And Sensory Neuropathy VI [MESH:C562851] (31)  Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 4E [MESH:C535301] (121)  Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Charcot-Marie-Tooth disease, Type 1D [MESH:C537985] (108)  Charcot-Marie-Tooth disease, Type 2B [MESH:C537989] (15)  Charcot-Marie-Tooth Disease, Axonal, Type 2A2 [MESH:C563757] (31)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 6, autosomal dominant [MESH:C536866] (12)  Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Spastic Paraplegia 42, Autosomal Dominant [MESH:C567262] (22)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Adrenoleukodystrophy [MESH:D000326] (1348)  Rett Syndrome [MESH:D015518] (143)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Pantothenate Kinase-Associated Neurodegeneration [MESH:D006211] (17)   Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration [MESH:C564603] (16)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar ataxia, autosomal recessive 1 [MESH:C537308] (21)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Xanthinuria, Type I [MESH:C562584] (190)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Methylmalonic acidemia [MESH:C537358] (764)  Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)   Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Muscular Dystrophies [MESH:D009136] (1597)   Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)  Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Familial cylindromatosis [MESH:C536611] (35)  Meningioma, familial [MESH:C537443] (195)  Birt-Hogg-Dube Syndrome [MESH:D058249] (35)  Exostoses, Multiple Hereditary [MESH:D005097] (154)  Skin Diseases, Genetic [MESH:D012873] (3456)   Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Cartilage Diseases [MESH:D002357] (438)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Scleroderma, Systemic [MESH:D012595] (199)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Noonan Syndrome [MESH:D009634] (506)   Noonan Syndrome 4 [MESH:C548082] (37)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Pruritus [MESH:D011537] (647)  Scleroderma, Systemic [MESH:D012595] (199)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Ulnar-mammary syndrome [MESH:C536937] (57)  Breast Neoplasms [MESH:D001943] (6077)   Carcinoma, Ductal, Breast [MESH:D018270] (1112)  Dermatitis [MESH:D003872] (4530)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  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)   Hypotrichosis [MESH:D007039] (1513)   Hypotrichosis simplex [MESH:C537160] (92)  Alopecia [MESH:D000505] (1453)  Pigmentation Disorders [MESH:D010859] (1215)   Hypopigmentation [MESH:D017496] (718)   Vitiligo [MESH:D014820] (504)  Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Skin Diseases, Eczematous [MESH:D017443] (3740)   Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Dermatitis, Contact [MESH:D003877] (3394)   Dermatitis, Allergic Contact [MESH:D017449] (3241)  Skin Diseases, Genetic [MESH:D012873] (3481)   Albinism [MESH:D000417] (359)   Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Skin Diseases, Infectious [MESH:D012874] (2684)   Skin Diseases, Parasitic [MESH:D012876] (2526)   Leishmaniasis [MESH:D007896] (2516)   Leishmaniasis, Cutaneous [MESH:D016773] (2359)  Skin Diseases, Viral [MESH:D017193] (203)   Warts [MESH:D014860] (172)   WHIM syndrome [MESH:C536697] (148)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Lichenoid Eruptions [MESH:D017512] (1324)  Psoriasis [MESH:D011565] (3278)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigoid, Bullous [MESH:D010391] (707)  Skin Neoplasms [MESH:D012878] (2991)   Familial cylindromatosis [MESH:C536611] (35)  Sweat Gland Diseases [MESH:D013543] (231)   Hyperhidrosis [MESH:D006945] (58)   Cold-Induced Sweating Syndrome 1 [MESH:C564791] (29) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Z. Exceptions (817)   Not Fully Specified [NFS] (817)  Metabolic Diseases [MESH:D008659] (9025)   Metabolic Syndrome X [MESH:D024821] (2151)  Acid-Base Imbalance [MESH:D000137] (854)   Acidosis [MESH:D000138] (626)   Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)   Aortic Valve, Calcification of [MESH:C562942] (655)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Diabetes Mellitus [MESH:D003920] (5891)   Maturity-Onset Diabetes of the Young, Type 7 [MESH:C566466] (32)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Hyperglycemia [MESH:D006943] (1858)   Glucose Intolerance [MESH:D018149] (605)  Hyperinsulinism [MESH:D006946] (3586)   Insulin Resistance [MESH:D007333] (3511)   Metabolic Syndrome X [MESH:D024821] (2151)  Iron Metabolism Disorders [MESH:D019189] (2139)   Neurodegeneration with brain iron accumulation (NBIA) [MESH:C538421] (30)  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)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Malabsorption Syndromes [MESH:D008286] (1869)   Celiac Disease [MESH:D002446] (340)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Xanthinuria, Type I [MESH:C562584] (190)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Methylmalonic acidemia [MESH:C537358] (764)  Albinism [MESH:D000417] (359)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Piebaldism [MESH:D016116] (167)  Albinism, Oculocutaneous [MESH:D016115] (234)   Hermanski-Pudlak Syndrome [MESH:D022861] (82)   Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells [MESH:C538539] (74)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Adrenoleukodystrophy [MESH:D000326] (1348)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1472)   Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Phenylketonurias [MESH:D010661] (156)   Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)  Urea Cycle Disorders, Inborn [MESH:D056806] (315)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid lipofuscinosis, neuronal 8 [MESH:C537952] (28)  Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Niemann-Pick Diseases [MESH:D009542] (136)   Niemann-Pick Disease, Type C [MESH:D052556] (103)  Peroxisomal Disorders [MESH:D018901] (1788)   Adrenoleukodystrophy [MESH:D000326] (1348)  Refsum Disease [MESH:D012035] (173)   Neuropathy, hereditary motor and sensory, LOM type [MESH:C535716] (131)  Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)   Acidosis, Renal Tubular [MESH:D000141] (225)   Osteopetrosis with renal tubular acidosis [MESH:C536058] (130)  Mitochondrial Diseases [MESH:D028361] (2561)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  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 4, Juvenile [MESH:C566550] (21)  Skin Diseases, Metabolic [MESH:D012875] (1574)   Lipodystrophy [MESH:D008060] (930)   Lipodystrophy, Familial Partial [MESH:D052496] (589)  Lipodystrophy, Congenital Generalized [MESH:D052497] (168)   Lipodystrophy, Congenital Generalized, Type 4 [MESH:C567642] (38)  Nutrition Disorders [MESH:D009748] (4945)   Overnutrition [MESH:D044343] (4463)   Obesity [MESH:D009765] (4462) C19. Endocrine System Diseases  C19. Endocrine System Diseases  Endocrine System Diseases [MESH:D004700] (8062)   Adrenal Gland Diseases [MESH:D000307] (2397)   Adrenal Insufficiency [MESH:D000309] (1599)   Adrenoleukodystrophy [MESH:D000326] (1348)  Diabetes Mellitus [MESH:D003920] (6159)   Maturity-Onset Diabetes of the Young, Type 7 [MESH:C566466] (32)  Diabetes, Gestational [MESH:D016640] (1152)  Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)   Wolcott-Rallison syndrome [MESH:C536739] (92)  Dwarfism [MESH:D004392] (698)   Desbuquois syndrome [MESH:C535943] (20)  Diastrophic dysplasia [MESH:C536170] (34)  Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Thyroid Neoplasms [MESH:D013964] (2040)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Gonadal Disorders [MESH:D006058] (5088)   Ovarian Diseases [MESH:D010049] (4253)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Testicular Diseases [MESH:D013733] (777)   Testicular Neoplasms [MESH:D013736] (520)   Testicular Germ Cell Tumor [MESH:C563236] (176)  Pituitary Diseases [MESH:D010900] (1829)   Hyperpituitarism [MESH:D006964] (1259)   Pituitary ACTH Hypersecretion [MESH:D047748] (599)  Thyroid Diseases [MESH:D013959] (2808)   Thyroid Neoplasms [MESH:D013964] (2040)  Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Glomerulonephritis, IGA [MESH:D005922] (897)  Graves Disease [MESH:D006111] (278)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Pemphigoid, Bullous [MESH:D010391] (707)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Nervous System Autoimmune Disease, Experimental [MESH:D020721] (810)   Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)   Wolcott-Rallison syndrome [MESH:C536739] (92)  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)   Eosinophilic Esophagitis [MESH:D057765] (43)  Dermatitis, Atopic [MESH:D003876] (2052)   Dermatitis, Atopic, 4 [MESH:C565291] (130)  Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Immune Complex Diseases [MESH:D007105] (782)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   WHIM syndrome [MESH:C536697] (148)  Agammaglobulinemia [MESH:D000361] (156)  HIV Infections [MESH:D015658] (3402)  Immunoproliferative Disorders [MESH:D007160] (4761)   Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, B-Cell [MESH:D015448] (2564)   Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor T-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054218] (510)  Lymphangiomyoma [MESH:D008203] (163)   Lymphangioleiomyomatosis [MESH:D018192] (162)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, B-Cell [MESH:D016393] (2624)   Burkitt Lymphoma [MESH:D002051] (691)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)   Alopecia [MESH:D000505] (1383)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Absent corpus callosum cataract immunodeficiency [MESH:C535566] (11)  Atrophy [MESH:D001284] (2603)   Muscular Atrophy [MESH:D009133] (1234)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Hypertrophy [MESH:D006984] (4476)   Hepatomegaly [MESH:D006529] (1169)  Cardiomegaly [MESH:D006332] (3802)   Hypertrophy, Left Ventricular [MESH:D017379] (1430)  Nails, Malformed [MESH:D009264] (184)   Witkop syndrome [MESH:C536736] (38)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Gliosis [MESH:D005911] (1419)  Growth Disorders [MESH:D006130] (2438)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Ulcer [MESH:D014456] (392)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Atrial Fibrillation [MESH:D001281] (1053)  Bradycardia [MESH:D001919] (1899)  Ventricular Fibrillation [MESH:D014693] (624)  Chromosome Aberrations [MESH:D002869] (2352)   Aneuploidy [MESH:D000782] (1237)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Recurrence [MESH:D012008] (830)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Fibrosis [MESH:D005355] (3133)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Cicatrix [MESH:D002921] (1115)   Keloid [MESH:D007627] (1110)  Hemorrhage [MESH:D006470] (4451)   Hematuria [MESH:D006417] (477)  Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)  Subarachnoid Hemorrhage [MESH:D013345] (1081)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Inflammation [MESH:D007249] (5241)   Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Shock, Septic [MESH:D012772] (1830)  Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)   Choroidal Neovascularization [MESH:D020256] (550)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm Recurrence, Local [MESH:D009364] (1949)  Carcinogenesis [MESH:D063646] (3391)   Cell Transformation, Neoplastic [MESH:D002471] (3389)  Neoplasm Metastasis [MESH:D009362] (4441)   Lymphatic Metastasis [MESH:D008207] (917)  Ossification, Heterotopic [MESH:D009999] (187)   Desbuquois syndrome [MESH:C535943] (20)  Postoperative Complications [MESH:D011183] (5311)   Graft Occlusion, Vascular [MESH:D006083] (139)  Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Shock [MESH:D012769] (2550)   Systemic Inflammatory Response Syndrome [MESH:D018746] (1832)   Shock, Septic [MESH:D012772] (1830)  Signs and Symptoms [MESH:D012816] (10659)   Edema [MESH:D004487] (3726)  Fatigue [MESH:D005221] (437)  Body Temperature Changes [MESH:D001832] (3130)   Fever [MESH:D005334] (2856)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)   Emaciation [MESH:D004614] (2285)   Cachexia [MESH:D002100] (2283)  Overweight [MESH:D050177] (4455)   Obesity [MESH:D009765] (4454)  Failure to Thrive [MESH:D005183] (415)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Neurologic Manifestations [MESH:D009461] (8702)   Seizures [MESH:D012640] (4502)  Dyskinesias [MESH:D020820] (3285)   Ataxia [MESH:D001259] (984)  Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tics [MESH:D020323] (62)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Memory Disorders [MESH:D008569] (3233)  Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Speech Disorders [MESH:D013064] (482)   Articulation Disorders [MESH:D001184] (164)   Dysarthria [MESH:D004401] (163)  Intellectual Disability [MESH:D008607] (1476)   Coffin-Siris syndrome [MESH:C536436] (102)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscular Atrophy [MESH:D009133] (1234)  Muscle Hypertonia [MESH:D009122] (775)   Muscle Rigidity [MESH:D009127] (617)  Pain [MESH:D010146] (3869)   Pain, Intractable [MESH:D010148] (707)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Paralysis [MESH:D010243] (2298)   Gastroparesis [MESH:D018589] (732)  Ophthalmoplegia [MESH:D009886] (1468)   Supranuclear Palsy, Progressive [MESH:D013494] (235)  Sensation Disorders [MESH:D012678] (5009)   Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Pain, Intractable [MESH:D010148] (707)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Angina, Unstable [MESH:D000789] (782)  Neuralgia [MESH:D009437] (2074)   Neuralgia, Postherpetic [MESH:D051474] (742)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Anorexia [MESH:D000855] (854)  Nausea [MESH:D009325] (2300)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Skin Manifestations [MESH:D012877] (1250)   Pruritus [MESH:D011537] (648)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Urological Manifestations [MESH:D020924] (3532)   Proteinuria [MESH:D011507] (3293)  Lower Urinary Tract Symptoms [MESH:D059411] (612)   Urinary Bladder, Overactive [MESH:D053201] (530) 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)  Dyskinesia, Drug-Induced [MESH:D004409] (1389)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Neurotoxicity Syndromes [MESH:D020258] (3323)   Dyskinesia, Drug-Induced [MESH:D004409] (1389)  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)  Opioid-Related Disorders [MESH:D009293] (1491)   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)   Heat Stress Disorders [MESH:D018882] (226)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  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) D01. Inorganic Chemicals  D01. Inorganic Chemicals  Coordination Complexes [MESH:D056831] (86) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Coordination Complexes [MESH:D056831] (86)  Organometallic Compounds [MESH:D009942] (4369)   Coordination Complexes [MESH:D056831] (86) 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)   Diagnostic Imaging [MESH:D003952] (623)   Ultrasonography [MESH:D014463] (482)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Diagnostic Techniques, Cardiovascular [MESH:D003935] (521)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)  Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407) 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)   Coffin-Siris syndrome [MESH:C536436] (102)  Mental Disorders [MESH:D001523] (2063)   Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Intellectual Disability [MESH:D008607] (1109)   Coffin-Siris syndrome [MESH:C536436] (102) 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)   5q- syndrome [MESH:C535323] (131)  Genetic Structures [MESH:D040342] (1612)   Chromosomes [MESH:D002875] (1304)   Chromosomes, Mammalian [MESH:D033481] (1282)   Chromosomes, Human [MESH:D002877] (1280)   Chromosomes, Human, 4-5 [MESH:D002905] (149)   Chromosomes, Human, Pair 5 [MESH:D002895] (136)   5q- syndrome [MESH:C535323] (131)  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)   5q- syndrome [MESH:C535323] (131)  Chromosome Aberrations [MESH:D002869] (1297)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Sequence Deletion [MESH:D017384] (1120)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Ploidies [MESH:D011003] (1227)   Aneuploidy [MESH:D000782] (1220)   Monosomy [MESH:D009006] (1121)   Chromosome Deletion [MESH:D002872] (1117)   5q- syndrome [MESH:C535323] (131)  Circulatory and Respiratory Physiological Phenomena [MESH:D002943] (614)   Cardiovascular Physiological Phenomena [MESH:D002320] (525)   Carotid Intima-Media Thickness [MESH:D059168] (458)   Carotid Intimal Medial Thickness 1 [MESH:C563733] (457)