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Current search: C23. Pathological Conditions, Signs and Symptoms: Pathological Conditions, Anatomical [MESH:D020763] > Cysts [MESH:D003560] > Leukoencephalopathy, Cystic, Without Megalencephaly [MESH:C567845] × Select any link to see items in a related category. more general categories    information about this item 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)  Urogenital System [MESH:D014566] (986)   Genitalia [MESH:D005835] (400)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Cardiovascular System [MESH:D002319] (1086)   Heart [MESH:D006321] (904)   Heart Atria [MESH:D006325] (65)   Atrial myxoma, familial [MESH:C538262] (34)  Cells [MESH:D002477] (1885)   Blood Cells [MESH:D001773] (196)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Cellular Structures [MESH:D022082] (1562)   Inclusion Bodies [MESH:D002479] (147)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127)  Hemic and Immune Systems [MESH:D006424] (272)   Blood [MESH:D001769] (200)   Blood Cells [MESH:D001773] (194)   Erythrocytes [MESH:D004912] (146)   Erythrocytes, Abnormal [MESH:D004913] (141)   Erythrocyte Inclusions [MESH:D004908] (129)   Heinz Bodies [MESH:D006366] (128)   Heinz Body Anemias [MESH:C563030] (127) C01. Bacterial Infections and Mycoses  C01. Bacterial Infections and Mycoses  Bacterial Infections [MESH:D001424] (3716)   Gram-Positive Bacterial Infections [MESH:D016908] (2434)   Actinomycetales Infections [MESH:D000193] (1466)   Mycobacterium Infections [MESH:D009164] (1446)   Paratuberculosis [MESH:D010283] (427)  Infection [MESH:D007239] (4109)   Sepsis [MESH:D018805] (3556)   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)   RNA Virus Infections [MESH:D012327] (4215)   Retroviridae Infections [MESH:D012192] (3420)   Lentivirus Infections [MESH:D016180] (3408)   HIV Infections [MESH:D015658] (3402)  Sexually Transmitted Diseases [MESH:D012749] (3305)   Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)   HIV Infections [MESH:D015658] (3296) C03. Parasitic Diseases  C03. Parasitic Diseases  Parasitic Diseases [MESH:D010272] (3828)   Liver Diseases, Parasitic [MESH:D008109] (1009)  Protozoan Infections [MESH:D011528] (3014)   Euglenozoa Infections [MESH:D056986] (2552)   Leishmaniasis [MESH:D007896] (2541)   Leishmaniasis, Visceral [MESH:D007898] (2149)  Malaria [MESH:D008288] (2175)   Malaria, Falciparum [MESH:D016778] (438) C04. Neoplasms  C04. Neoplasms  Neoplasms [MESH:D009369] (10293)   Precancerous Conditions [MESH:D011230] (2858)  Cysts [MESH:D003560] (2625)   Leukoencephalopathy, Cystic, Without Megalencephaly [MESH:C567845] (25)  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, T-Cell [MESH:D015458] (395)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Leukemia, Myeloid [MESH:D007951] (2773)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Leukemia, Myeloid, Acute [MESH:D015470] (2176)   Leukemia, Promyelocytic, Acute [MESH:D015473] (1367)  Lymphoma [MESH:D008223] (3686)   Lymphoma, Non-Hodgkin [MESH:D008228] (3337)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1405)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Neoplasms, Complex and Mixed [MESH:D018193] (1121)   Carcinosarcoma [MESH:D002296] (581)  Rhabdoid Tumor [MESH:D018335] (61)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)   Neoplasms, Connective Tissue [MESH:D009372] (3626)   Sarcoma, Synovial [MESH:D013584] (993)  Chondroma [MESH:D002812] (155)   Chondromatosis [MESH:D018210] (52)   Metachondromatosis [MESH:C562938] (49)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Myxoma [MESH:D009232] (78)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Neoplasms, Bone Tissue [MESH:D018213] (2217)   Osteosarcoma [MESH:D012516] (2175)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Metachondromatosis [MESH:C562938] (49)  Neoplasms, Muscle Tissue [MESH:D009379] (1965)   Leiomyoma [MESH:D007889] (744)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Sarcoma [MESH:D012509] (4246)   Carcinosarcoma [MESH:D002296] (581)  Hemangiosarcoma [MESH:D006394] (1836)  Osteosarcoma [MESH:D012516] (2175)  Sarcoma, Synovial [MESH:D013584] (993)  Chondrosarcoma [MESH:D002813] (1217)   Chondrosarcoma, Mesenchymal [MESH:D018211] (1161)  Myosarcoma [MESH:D009217] (790)   Rhabdomyosarcoma [MESH:D012208] (789)  Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)   Neuroectodermal Tumors [MESH:D017599] (5066)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3633)   Melanoma [MESH:D008545] (3508)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)   Adenoma [MESH:D000236] (4051)   Adenoma, Liver Cell [MESH:D018248] (685)  Adenoma, Oxyphilic [MESH:D018249] (115)  Mesothelioma [MESH:D008654] (2567)  Carcinoma [MESH:D002277] (7263)   Thyroid cancer, papillary [MESH:C536915] (111)  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)  Cholangiocarcinoma [MESH:D018281] (2398)  Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Carcinoma in Situ [MESH:D002278] (2111)   Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565)  Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)   Carcinoma, Ductal [MESH:D044584] (1786)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Neoplasms, Mesothelial [MESH:D018301] (2569)   Mesothelioma [MESH:D008654] (2567)  Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neoplasms, Squamous Cell [MESH:D018307] (4457)   Carcinoma, Squamous Cell [MESH:D002294] (4294)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Neoplasms, Nerve Tissue [MESH:D009380] (5201)   Neuroectodermal Tumors [MESH:D017599] (5059)   Neoplasms, Neuroepithelial [MESH:D018302] (4487)   Glioma [MESH:D005910] (4261)   Medulloblastoma [MESH:D008527] (1282)  Oligodendroglioma [MESH:D009837] (241)  Astrocytoma [MESH:D001254] (2692)   Glioblastoma [MESH:D005909] (2554)  Neuroectodermal Tumors, Primitive [MESH:D018242] (2005)   Medulloblastoma [MESH:D008527] (1282)  Neuroectodermal Tumors, Primitive, Peripheral [MESH:D018241] (1433)   Neuroblastoma [MESH:D009447] (1420)  Neuroendocrine Tumors [MESH:D018358] (3625)   Melanoma [MESH:D008545] (3508)  Paraganglioma [MESH:D010235] (297)   Pheochromocytoma [MESH:D010673] (275)  Neoplasms, Plasma Cell [MESH:D054219] (2772)   Multiple Myeloma [MESH:D009101] (2767)  Neoplasms, Vascular Tissue [MESH:D009383] (2959)   Hemangiosarcoma [MESH:D006394] (1836)  Nevi and Melanomas [MESH:D018326] (3572)   Melanoma [MESH:D008545] (3508)  Nevus [MESH:D009506] (340)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neoplasms by Site [MESH:D009371] (9169)   Breast Neoplasms [MESH:D001943] (6077)  Bone Neoplasms [MESH:D001859] (1334)   Metachondromatosis [MESH:C562938] (49)  Digestive System Neoplasms [MESH:D004067] (7487)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6452)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5358)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  Carcinoma, Hepatocellular [MESH:D006528] (5375)  Liver Neoplasms, Experimental [MESH:D008114] (2837)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  Head and Neck Neoplasms [MESH:D006258] (4612)   Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  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)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Thoracic Neoplasms [MESH:D013899] (6032)   Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  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)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Neoplasms, Experimental [MESH:D009374] (5218)   Liver Neoplasms, Experimental [MESH:D008114] (2837)  Mammary Neoplasms, Experimental [MESH:D008325] (3268)  Neoplastic Processes [MESH:D009385] (5317)   Neoplasm Invasiveness [MESH:D009361] (3388)  Neoplasm 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)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Metachondromatosis [MESH:C562938] (49) C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Bone Diseases [MESH:D001847] (5801)   Bone Diseases, Developmental [MESH:D001848] (3315)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Dysostoses [MESH:D004413] (1019)  Osteochondrodysplasias [MESH:D010009] (2440)   Epiphyseal dysplasia, multiple, 2 [MESH:C535502] (18)  Enchondromatosis [MESH:D004687] (170)  Osteochondroma [MESH:D015831] (157)   Osteochondromatosis [MESH:D018216] (155)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Metachondromatosis [MESH:C562938] (49)  Osteosclerosis [MESH:D010026] (356)   Melorheostosis [MESH:D008557] (12)  Osteopetrosis [MESH:D010022] (318)  Osteopoikilosis [MESH:D010023] (15)   Buschke-Ollendorff syndrome [MESH:C537415] (11)  Bone Diseases, Metabolic [MESH:D001851] (3492)   Osteoporosis [MESH:D010024] (3037)  Bone Neoplasms [MESH:D001859] (1334)   Metachondromatosis [MESH:C562938] (49)  Hyperostosis [MESH:D015576] (493)   Exostoses [MESH:D005096] (160)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Metachondromatosis [MESH:C562938] (49)  Spinal Diseases [MESH:D013122] (2485)   Intervertebral Disc Degeneration [MESH:D055959] (827)   Intervertebral disc disease [MESH:C535531] (514)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Spondylitis [MESH:D013166] (1924)   Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  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)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Joint Diseases [MESH:D007592] (4657)   Synovitis [MESH:D013585] (270)  Ankylosis [MESH:D000844] (479)   Spondylitis, Ankylosing [MESH:D013167] (431)  Arthritis [MESH:D001168] (4416)   Arthritis, Experimental [MESH:D001169] (3142)  Arthritis, Psoriatic [MESH:D015535] (1859)  Arthritis, Rheumatoid [MESH:D001172] (3603)  Osteoarthritis [MESH:D010003] (1743)  Spondylarthritis [MESH:D025241] (1912)   Spondylarthropathies [MESH:D025242] (1909)   Arthritis, Psoriatic [MESH:D015535] (1859)  Spondylitis, Ankylosing [MESH:D013167] (431)  Muscular Diseases [MESH:D009135] (4071)   Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)  Myopathies, Structural, Congenital [MESH:D020914] (272)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Muscular Disorders, Atrophic [MESH:D020966] (1598)   Muscular Dystrophies [MESH:D009136] (1593)   Distal Myopathies [MESH:D049310] (178)  Myositis [MESH:D009220] (2071)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Costello Syndrome [MESH:D056685] (407)  LEOPARD Syndrome [MESH:D044542] (299)  Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Microcephaly [MESH:D008831] (700)   Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Limb Deformities, Congenital [MESH:D017880] (1813)   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)  Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gallbladder Diseases [MESH:D005705] (1215)   Gallbladder Neoplasms [MESH:D005706] (993)  Digestive System Abnormalities [MESH:D004065] (2127)   Anus, Imperforate [MESH:D001006] (140)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Digestive System Neoplasms [MESH:D004067] (7493)   Biliary Tract Neoplasms [MESH:D001661] (1165)   Gallbladder Neoplasms [MESH:D005706] (993)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  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)   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)  Gastroenteritis [MESH:D005759] (4066)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Gastrointestinal Neoplasms [MESH:D005770] (6460)   Stomach Neoplasms [MESH:D013274] (4942)  Esophageal Neoplasms [MESH:D004938] (3737)   Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Intestinal Diseases [MESH:D007410] (6206)   Cecal Diseases [MESH:D002429] (1330)   Cecal Neoplasms [MESH:D002430] (822)  Colonic Diseases [MESH:D003108] (5564)   Colitis [MESH:D003092] (3199)   Colitis, Ulcerative [MESH:D003093] (2601)  Colorectal Neoplasms [MESH:D015179] (5282)   Colonic Neoplasms [MESH:D003110] (4405)  Inflammatory Bowel Diseases [MESH:D015212] (3492)   Colitis, Ulcerative [MESH:D003093] (2601)  Intestinal Neoplasms [MESH:D007414] (5359)   Cecal Neoplasms [MESH:D002430] (822)  Colorectal Neoplasms [MESH:D015179] (5294)   Colonic Neoplasms [MESH:D003110] (4405)  Rectal Diseases [MESH:D012002] (4596)   Colorectal Neoplasms [MESH:D015179] (4534)  Stomach Diseases [MESH:D013272] (5325)   Stomach Neoplasms [MESH:D013274] (4942)  Liver Diseases [MESH:D008107] (8167)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Fatty Liver [MESH:D005234] (3584)  Hepatitis [MESH:D006505] (3883)  Hepatolenticular Degeneration [MESH:D006527] (473)  Liver Cirrhosis [MESH:D008103] (5542)  Liver Diseases, Alcoholic [MESH:D008108] (3243)  Liver Diseases, Parasitic [MESH:D008109] (1009)  Hepatic Insufficiency [MESH:D048550] (2771)   Liver Failure [MESH:D017093] (2768)   Liver Failure, Acute [MESH:D017114] (2404)  Liver Neoplasms [MESH:D008113] (6048)   Adenoma, Liver Cell [MESH:D018248] (685)  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)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Diseases [MESH:D009059] (4783)   Behcet Syndrome [MESH:D001528] (1784)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Mouth Neoplasms [MESH:D009062] (2263)   Salivary Gland Neoplasms [MESH:D012468] (968)  Tongue Neoplasms [MESH:D014062] (1518)  Salivary Gland Diseases [MESH:D012466] (1213)   Salivary Gland Neoplasms [MESH:D012468] (968)  Sialorrhea [MESH:D012798] (252)  Stomatitis [MESH:D013280] (1235)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Tongue Diseases [MESH:D014060] (1544)   Tongue Neoplasms [MESH:D014062] (1518)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65) C08. Respiratory Tract Diseases  C08. Respiratory Tract Diseases  Respiratory Tract Diseases [MESH:D012140] (7881)   Bronchial Diseases [MESH:D001982] (4382)   Asthma [MESH:D001249] (4098)  Bronchial Hyperreactivity [MESH:D016535] (1357)  Bronchiectasis [MESH:D001987] (1792)  Lung Diseases [MESH:D008171] (7249)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Pneumonia [MESH:D011014] (3482)  Pulmonary Fibrosis [MESH:D011658] (3140)  Lung Diseases, Interstitial [MESH:D017563] (2966)   Pneumoconiosis [MESH:D011009] (2789)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Lung Diseases, Obstructive [MESH:D008173] (4697)   Asthma [MESH:D001249] (3903)  Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564)   Pulmonary Emphysema [MESH:D011656] (1259)  Lung Injury [MESH:D055370] (3688)   Pneumoconiosis [MESH:D011009] (2789)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  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)  Respiration Disorders [MESH:D012120] (2218)   Hyperventilation [MESH:D006985] (654)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Respiratory Hypersensitivity [MESH:D012130] (4401)   Asthma [MESH:D001249] (4098)  Respiratory Tract Infections [MESH:D012141] (3926)   Pneumonia [MESH:D011014] (3482)  Respiratory Tract Neoplasms [MESH:D012142] (6053)   Lung Neoplasms [MESH:D008175] (6013)   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)   Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227) C10. Nervous System Diseases  C10. Nervous System Diseases  Z. Exceptions (4027)   Not Fully Specified [NFS] (4027)  Nervous System Diseases [MESH:D009422] (13325)   Restless Legs Syndrome [MESH:D012148] (379)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Central Nervous System Diseases [MESH:D002493] (9745)   Brain Diseases [MESH:D001927] (9294)   Brain Injuries [MESH:D001930] (3429)  Hypoxia, Brain [MESH:D002534] (134)  Basal Ganglia Diseases [MESH:D001480] (4268)   Hepatolenticular Degeneration [MESH:D006527] (473)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 6, Autosomal Recessive Early-Onset [MESH:C565276] (42)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Brain Diseases, Metabolic [MESH:D001928] (3351)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Alexander Disease [MESH:D038261] (168)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Brain Neoplasms [MESH:D001932] (2764)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Cerebellar Diseases [MESH:D002526] (736)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Cerebrovascular Disorders [MESH:D002561] (5542)   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)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2463)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  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)   Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Epilepsy [MESH:D004827] (6274)   Mental Retardation, X-Linked, with Epilepsy [MESH:C564516] (34)  Epilepsy, Benign Neonatal [MESH:D020936] (57)  Seizures [MESH:D012640] (4502)  Status Epilepticus [MESH:D013226] (4014)  Epilepsies, Myoclonic [MESH:D004831] (1344)   Familial encephalopathy with neuroserpin inclusion bodies [MESH:C536841] (40)  Epilepsies, Partial [MESH:D004828] (1267)   Cortical Dysplasia-Focal Epilepsy Syndrome [MESH:C566482] (24)  Epilepsy, Generalized [MESH:D004829] (1431)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Epilepsy, Tonic-Clonic [MESH:D004830] (1042)  Seizures, Febrile [MESH:D003294] (229)   Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170)  Headache Disorders [MESH:D020773] (2337)   Headache Disorders, Primary [MESH:D051270] (2327)   Migraine Disorders [MESH:D008881] (2318)   Migraine without Aura [MESH:D020326] (408)  Leukoencephalopathies [MESH:D056784] (1916)   Leukoencephalopathy, Cystic, Without Megalencephaly [MESH:C567845] (25)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Alexander Disease [MESH:D038261] (168)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Central Nervous System Infections [MESH:D002494] (1823)   Prion Diseases [MESH:D017096] (488)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Creutzfeldt-Jakob Syndrome [MESH:D007562] (118)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Movement Disorders [MESH:D009069] (4823)   Hepatolenticular Degeneration [MESH:D006527] (473)  Dyskinesias [MESH:D020820] (1827)   Chorea [MESH:D002819] (651)   Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dystonic Disorders [MESH:D020821] (729)   Juvenile-onset dystonia [MESH:C537704] (143)  Parkinsonian Disorders [MESH:D020734] (4009)   Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 6, Autosomal Recessive Early-Onset [MESH:C565276] (42)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  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)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Chronobiology Disorders [MESH:D021081] (970)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)  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)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  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)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  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)  Alexander Disease [MESH:D038261] (168)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Cortical Dysplasia-Focal Epilepsy Syndrome [MESH:C566482] (24)  Neuronal Migration Disorders [MESH:D054081] (264)  Microcephaly [MESH:D008831] (700)   Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Nervous System Neoplasms [MESH:D009423] (3073)   Central Nervous System Neoplasms [MESH:D016543] (3055)   Brain Neoplasms [MESH:D001932] (2764)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Neurocutaneous Syndromes [MESH:D020752] (1230)   Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Neurodegenerative Diseases [MESH:D019636] (6613)   Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)   Familial encephalopathy with neuroserpin inclusion bodies [MESH:C536841] (40)  Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Alexander Disease [MESH:D038261] (168)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 2 [MESH:C566857] (39)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Lewy Body Disease [MESH:D020961] (1143)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular Atrophy, Spinal [MESH:D009134] (850)   Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219)  Parkinson Disease [MESH:D010300] (3595)   Parkinson Disease 6, Autosomal Recessive Early-Onset [MESH:C565276] (42)  Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Prion Diseases [MESH:D017096] (475)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Insomnia, Fatal Familial [MESH:D034062] (98)  Scrapie [MESH:D012608] (462)  Tauopathies [MESH:D024801] (4289)   Alzheimer Disease [MESH:D000544] (4275)   Alzheimer disease type 2 [MESH:C536595] (165)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Neurologic Manifestations [MESH:D009461] (8964)   Neurogenic Inflammation [MESH:D020078] (2246)  Seizures [MESH:D012640] (4514)  Dyskinesias [MESH:D020820] (3365)   Dystonia [MESH:D004421] (848)  Hyperkinesis [MESH:D006948] (1799)  Hypokinesia [MESH:D018476] (279)  Tics [MESH:D020323] (62)  Tremor [MESH:D014202] (840)  Ataxia [MESH:D001259] (1138)   Cerebellar Ataxia [MESH:D002524] (542)   Spinocerebellar Ataxias [MESH:D020754] (406)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Neurobehavioral Manifestations [MESH:D019954] (5230)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Stuttering [MESH:D013342] (38)  Consciousness Disorders [MESH:D003244] (680)   Unconsciousness [MESH:D014474] (660)   Coma [MESH:D003128] (524)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (3054)   Coffin-Siris syndrome [MESH:C536436] (102)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Cri-du-Chat Syndrome [MESH:D003410] (139)  Mental Retardation, X-Linked [MESH:D038901] (1854)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Mental Retardation, X-Linked 30 [MESH:C563146] (40)  Mental Retardation, X-Linked, with Epilepsy [MESH:C564516] (34)  Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Coffin-Lowry Syndrome [MESH:D038921] (45)  Fragile X Syndrome [MESH:D005600] (353)  Psychomotor Disorders [MESH:D011596] (576)   Bowen-Conradi syndrome [MESH:C537081] (18)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)  Spasm [MESH:D013035] (418)  Muscle Hypotonia [MESH:D009123] (258)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Pain [MESH:D010146] (3875)   Headache [MESH:D006261] (1416)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Reflex, Abnormal [MESH:D012021] (485)   Reflex, Babinski [MESH:D001405] (97)  Sensation Disorders [MESH:D012678] (5011)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2103)   Hearing Loss [MESH:D034381] (2068)   Hearing Loss, Sensorineural [MESH:D006319] (1227)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Neuromuscular Diseases [MESH:D009468] (7336)   Motor Neuron Disease [MESH:D016472] (3670)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Muscular 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)   Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)  Myopathies, Structural, Congenital [MESH:D020914] (272)  Muscular Disorders, Atrophic [MESH:D020966] (1594)   Muscular Dystrophies [MESH:D009136] (1589)   Distal Myopathies [MESH:D049310] (178)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Myositis [MESH:D009220] (2069)   Dermatomyositis [MESH:D003882] (1826)  Polymyositis [MESH:D017285] (2007)   Dermatomyositis [MESH:D003882] (1826)  Neuromuscular Junction Diseases [MESH:D020511] (712)   Myasthenia Gravis [MESH:D009157] (632)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Myopathy, Congenital, Compton-North [MESH:C567261] (35)  Peripheral Nervous System Diseases [MESH:D010523] (6151)   Neuralgia [MESH:D009437] (2078)  Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Mononeuropathies [MESH:D020422] (604)   Median Neuropathy [MESH:D020423] (153)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Nerve Compression Syndromes [MESH:D009408] (166)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Polyneuropathies [MESH:D011115] (1134)   Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Neurotoxicity Syndromes [MESH:D020258] (4570)   Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)   Arsenic Poisoning [MESH:D020261] (2540)  Manganese Poisoning [MESH:D020149] (2214)  Sleep Disorders [MESH:D012893] (2050)   Dyssomnias [MESH:D020920] (1417)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (94)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)  Sleep Disorders, Intrinsic [MESH:D020919] (1270)   Restless Legs Syndrome [MESH:D012148] (379)  Disorders of Excessive Somnolence [MESH:D006970] (581)   Narcolepsy [MESH:D009290] (478)  Sleep Initiation and Maintenance Disorders [MESH:D007319] (354)   Insomnia, Fatal Familial [MESH:D034062] (98)  Parasomnias [MESH:D020447] (453)   Restless Legs Syndrome [MESH:D012148] (379)  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 Dystrophies, Hereditary [MESH:D003317] (341)   Doyne honeycomb retinal dystrophy [MESH:C535602] (44)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Eye Diseases, Hereditary [MESH:D015785] (1869)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Retinitis Pigmentosa [MESH:D012174] (414)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Doyne honeycomb retinal dystrophy [MESH:C535602] (44)  Lens Diseases [MESH:D007905] (900)   Cataract [MESH:D002386] (860)  Ocular Motility Disorders [MESH:D015835] (1699)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  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 Degeneration [MESH:D012162] (2386)   Macular Degeneration [MESH:D008268] (995)   Macular Degeneration, Age-Related, 7 [MESH:C565718] (60)  Macular Degeneration, Age-Related, 1 [MESH:C566411] (276)  Macular Degeneration, Age-Related, 9 [MESH:C566958] (149)  Retinal Dystrophies [MESH:D058499] (1315)   Retinitis Pigmentosa [MESH:D012174] (1307)  Uveal Diseases [MESH:D014603] (2428)   Uveitis [MESH:D014605] (2157)   Panuveitis [MESH:D015864] (1805)   Uveitis, Anterior [MESH:D014606] (1791)   Behcet Syndrome [MESH:D001528] (1784) C12. Male Urogenital Diseases  C12. Male Urogenital Diseases  Male Urogenital Diseases [MESH:D052801] (8891)   Genital Diseases, Male [MESH:D005832] (6794)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Infertility [MESH:D007246] (2909)   Infertility, Male [MESH:D007248] (2851)  Penile Diseases [MESH:D010409] (1805)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Diseases [MESH:D011469] (6204)   Prostatic Neoplasms [MESH:D011471] (6135)  Testicular Diseases [MESH:D013733] (451)   Cryptorchidism [MESH:D003456] (215)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Urogenital Abnormalities [MESH:D014564] (2065)   Cryptorchidism [MESH:D003456] (215)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Urogenital Neoplasms [MESH:D014565] (6932)   Genital Neoplasms, Male [MESH:D005834] (6224)   Penile Neoplasms [MESH:D010412] (890)  Prostatic Neoplasms [MESH:D011471] (6135)  Urologic Neoplasms [MESH:D014571] (5315)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Kidney Neoplasms [MESH:D007680] (3966)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7792)   Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Diabetic Nephropathies [MESH:D003928] (2301)  Kidney Neoplasms [MESH:D007680] (3966)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Urinary Bladder Diseases [MESH:D001745] (4374)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455) C13. Female Urogenital Diseases and Pregnancy Complications  C13. Female Urogenital Diseases and Pregnancy Complications  Female Urogenital Diseases [MESH:D052776] (8724)   Genital Diseases, Female [MESH:D005831] (5563)   Endometriosis [MESH:D004715] (2461)  Adnexal Diseases [MESH:D000291] (4273)   Ovarian Diseases [MESH:D010049] (4255)   Ovarian Neoplasms [MESH:D010051] (3281)  Ovarian Cysts [MESH:D010048] (2534)   Polycystic Ovary Syndrome [MESH:D011085] (2186)  Uterine Diseases [MESH:D014591] (2479)   Uterine Neoplasms [MESH:D014594] (2430)   Endometrial Neoplasms [MESH:D016889] (1984)  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)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Urologic Diseases [MESH:D014570] (7793)   Kidney Diseases [MESH:D007674] (7242)   Lipoprotein Glomerulopathy [MESH:C567089] (165)  Diabetic Nephropathies [MESH:D003928] (2301)  Kidney Neoplasms [MESH:D007680] (3966)   Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23)  Carcinoma, Renal Cell [MESH:D002292] (2975)  Nephritis [MESH:D009393] (4236)   Glomerulonephritis [MESH:D005921] (3758)   Glomerulonephritis, Membranous [MESH:D015433] (642)  Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)  Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Nephrosis [MESH:D009401] (2228)   Nephrotic Syndrome [MESH:D009404] (1536)  Renal Insufficiency [MESH:D051437] (4951)   Acute Kidney Injury [MESH:D058186] (4142)  Uremia [MESH:D014511] (2898)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Urinary Bladder Diseases [MESH:D001745] (4375)   Urinary Bladder Neoplasms [MESH:D001749] (4079)  Urination Disorders [MESH:D014555] (3598)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57)  Urolithiasis [MESH:D052878] (585)   Nephrolithiasis [MESH:D053040] (492)   Kidney Calculi [MESH:D007669] (455)  Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Pregnancy Complications [MESH:D011248] (4768)   Fetal Death [MESH:D005313] (464)  Abortion, Spontaneous [MESH:D000022] (2780)   Embryo Loss [MESH:D020964] (288)  Fetal Diseases [MESH:D005315] (1206)   Fetal Growth Retardation [MESH:D005317] (986)   Bowen-Conradi syndrome [MESH:C537081] (18)  Hypertension, Pregnancy-Induced [MESH:D046110] (1453)   Pre-Eclampsia [MESH:D011225] (1435) C14. Cardiovascular Diseases  C14. Cardiovascular Diseases  Z. Exceptions (2667)   Not Fully Specified [NFS] (2667)  Cardiovascular Diseases [MESH:D002318] (10123)   Cardiovascular Abnormalities [MESH:D018376] (3153)   Heart Defects, Congenital [MESH:D006330] (2447)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Heart Diseases [MESH:D006331] (8614)   Glycogen Storage Disease of Heart, Lethal Congenital [MESH:C564888] (30)  Heart Failure [MESH:D006333] (4058)  Arrhythmias, Cardiac [MESH:D001145] (4679)   Cardiac Arrhythmia, Ankyrin-B-Related [MESH:C566996] (32)  Bradycardia [MESH:D001919] (1899)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 2 [MESH:C567087] (15)  Brugada Syndrome 5 [MESH:C567556] (37)  Pre-Excitation Syndromes [MESH:D011226] (43)   Wolff-Parkinson-White Syndrome [MESH:D014927] (40)  Cardiomegaly [MESH:D006332] (4081)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Cardiomyopathies [MESH:D009202] (5331)   Cardiomyopathy, Dilated [MESH:D002311] (1576)  Diabetic Cardiomyopathies [MESH:D058065] (1995)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)   Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 6 [MESH:C563436] (30)  Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Heart Defects, Congenital [MESH:D006330] (2443)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  LEOPARD Syndrome [MESH:D044542] (299)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Heart Neoplasms [MESH:D006338] (47)   Atrial myxoma, familial [MESH:C538262] (34)  Carney Complex [MESH:D056733] (45)  Heart Valve Diseases [MESH:D006349] (3333)   Aortic Valve Stenosis [MESH:D001024] (1742)   Aortic Stenosis, Subvalvular [MESH:D001020] (1455)   Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)  Pulmonary Valve Stenosis [MESH:D011666] (360)   LEOPARD Syndrome [MESH:D044542] (299)  Myocardial Ischemia [MESH:D017202] (5787)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4122)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  Vascular Diseases [MESH:D014652] (8691)   Angioedema [MESH:D000799] (837)  Hyperemia [MESH:D006940] (2372)  Hypertension [MESH:D006973] (5655)  Hypotension [MESH:D007022] (4045)  Vascular System Injuries [MESH:D057772] (2086)  Arterial Occlusive Diseases [MESH:D001157] (4520)   Carotid Stenosis [MESH:D016893] (174)  Arteriosclerosis [MESH:D001161] (4466)   Atherosclerosis [MESH:D050197] (4188)  Coronary Artery Disease [MESH:D003324] (2685)  Cerebrovascular Disorders [MESH:D002561] (5541)   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)  Carotid Artery Diseases [MESH:D002340] (1993)   Carotid Stenosis [MESH:D016893] (174)  Cerebral Small Vessel Diseases [MESH:D059345] (1292)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Arterial Diseases [MESH:D020765] (2468)   Cerebral Arterial Diseases [MESH:D002539] (2440)   Infarction, Middle Cerebral Artery [MESH:D020244] (2268)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Intracranial Hemorrhages [MESH:D020300] (3269)   Cerebral Hemorrhage [MESH:D002543] (2873)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  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)  Hemostatic Disorders [MESH:D020141] (2894)   Multiple Myeloma [MESH:D009101] (2765)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Myocardial Ischemia [MESH:D017202] (5791)   Acute Coronary Syndrome [MESH:D054058] (2286)  Myocardial Infarction [MESH:D009203] (4151)  Myocardial Reperfusion Injury [MESH:D015428] (3500)  Angina Pectoris [MESH:D000787] (2575)   Acute Coronary Syndrome [MESH:D054058] (2286)  Coronary Disease [MESH:D003327] (3439)   Coronary Artery Disease [MESH:D003324] (2685)  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)   Methemoglobinemia [MESH:D008708] (850)  Polycythemia [MESH:D011086] (412)  Anemia [MESH:D000740] (3966)   Anemia, Hemolytic [MESH:D000743] (3083)   CD59 Deficiency [MESH:C567355] (57)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  beta-Thalassemia [MESH:D017086] (458)  Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Anemia, Hypochromic [MESH:D000747] (616)   Anemia, hypochromic microcytic [MESH:C536357] (164)  Blood Coagulation Disorders [MESH:D001778] (1828)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Blood Platelet Disorders [MESH:D001791] (3174)   Thrombocytopenia [MESH:D013921] (2966)   Thrombotic Microangiopathies [MESH:D057049] (2598)   Hemolytic-Uremic Syndrome [MESH:D006463] (2435)   Atypical hemolytic uremic syndrome [MESH:C538266] (277)  Blood Protein Disorders [MESH:D001796] (3051)   Hypergammaglobulinemia [MESH:D006942] (137)  Paraproteinemias [MESH:D010265] (2781)   Multiple Myeloma [MESH:D009101] (2765)  Bone Marrow Diseases [MESH:D001855] (2944)   Myelodysplastic Syndromes [MESH:D009190] (2093)  Myelodysplastic-Myeloproliferative Diseases [MESH:D054437] (376)   Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344)  Myeloproliferative Disorders [MESH:D009196] (1492)   Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032)  Polycythemia Vera [MESH:D011087] (244)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  beta-Thalassemia [MESH:D017086] (458)  Hemorrhagic Disorders [MESH:D006474] (3359)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Hemostatic Disorders [MESH:D020141] (2932)   Multiple Myeloma [MESH:D009101] (2765)  Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Leukocyte Disorders [MESH:D007960] (2662)   Eosinophilia [MESH:D004802] (537)   Eosinophilia-Myalgia Syndrome [MESH:D016603] (31)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (998)   Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Thrombophilia [MESH:D019851] (592)   Disseminated Intravascular Coagulation [MESH:D004211] (462)  Lymphatic Diseases [MESH:D008206] (5167)   Histiocytosis [MESH:D015614] (336)   Histiocytosis, Non-Langerhans-Cell [MESH:D015616] (315)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Lymphoproliferative Disorders [MESH:D008232] (4638)   Sarcoidosis [MESH:D012507] (895)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities  Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)   Congenital Abnormalities [MESH:D000013] (8109)   Abnormalities, Multiple [MESH:D000015] (3192)   Coffin-Siris syndrome [MESH:C536436] (102)  Carney Complex [MESH:D056733] (45)  Costello Syndrome [MESH:D056685] (407)  Cri-du-Chat Syndrome [MESH:D003410] (139)  LEOPARD Syndrome [MESH:D044542] (299)  Nevus, Sebaceous of Jadassohn [MESH:D054000] (209)  Ectodermal Dysplasia [MESH:D004476] (938)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Cardiovascular Abnormalities [MESH:D018376] (3294)   Heart Defects, Congenital [MESH:D006330] (2611)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  LEOPARD Syndrome [MESH:D044542] (299)  Wolff-Parkinson-White Syndrome [MESH:D014927] (40)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Chromosome Disorders [MESH:D025063] (2030)   Cri-du-Chat Syndrome [MESH:D003410] (139)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Digestive System Abnormalities [MESH:D004065] (507)   Anus, Imperforate [MESH:D001006] (140)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Eye Abnormalities [MESH:D005124] (1233)   Coloboma [MESH:D003103] (315)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   LEOPARD Syndrome [MESH:D044542] (299)  Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Microcephaly [MESH:D008831] (700)   Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Limb Deformities, Congenital [MESH:D017880] (1813)   Hand Deformities, Congenital [MESH:D006228] (587)   Coffin-Siris syndrome [MESH:C536436] (102)  Nervous System Malformations [MESH:D009421] (3354)   Agenesis of Corpus Callosum [MESH:D061085] (345)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Malformations of Cortical Development [MESH:D054220] (1406)   Cortical Dysplasia-Focal Epilepsy Syndrome [MESH:C566482] (24)  Neuronal Migration Disorders [MESH:D054081] (264)  Microcephaly [MESH:D008831] (700)   Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Neural Tube Defects [MESH:D009436] (2143)   Spinal Dysraphism [MESH:D016135] (1025)   Spina Bifida Cystica [MESH:D016137] (209)  Skin Abnormalities [MESH:D012868] (1723)   Carney Complex [MESH:D056733] (45)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Micrognathism [MESH:D008844] (230)   Coffin-Siris syndrome [MESH:C536436] (102)  Mouth Abnormalities [MESH:D009056] (1383)   Cleft Palate [MESH:D002972] (1330)   Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Urogenital Abnormalities [MESH:D014564] (2064)   Cryptorchidism [MESH:D003456] (215)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Fetal Diseases [MESH:D005315] (1205)   Fetal Growth Retardation [MESH:D005317] (986)   Bowen-Conradi syndrome [MESH:C537081] (18)  Genetic Diseases, Inborn [MESH:D030342] (9766)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  Costello Syndrome [MESH:D056685] (407)  Anemia, Hemolytic, Congenital [MESH:D000745] (2001)   Heinz Body Anemias [MESH:C563030] (127)  Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (501)   alpha-Thalassemia [MESH:D017085] (176)  beta-Thalassemia [MESH:D017086] (458)  Brugada Syndrome [MESH:D053840] (195)   Brugada Syndrome 2 [MESH:C567087] (15)  Brugada Syndrome 5 [MESH:C567556] (37)  Cardiomyopathy, Hypertrophic, Familial [MESH:D024741] (339)   Cardiomyopathy, Familial Hypertrophic, 6 [MESH:C563436] (30)  Cardiomyopathy, Familial Hypertrophic, 1 [MESH:C566005] (190)  Chromosome Disorders [MESH:D025063] (2030)   Cri-du-Chat Syndrome [MESH:D003410] (139)  Sex Chromosome Disorders [MESH:D025064] (479)   Fragile X Syndrome [MESH:D005600] (353)  Eye Diseases, Hereditary [MESH:D015785] (1867)   Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement [MESH:C567572] (70)  Retinitis Pigmentosa [MESH:D012174] (442)  Corneal Dystrophies, Hereditary [MESH:D003317] (341)   Doyne honeycomb retinal dystrophy [MESH:C535602] (44)  Genetic Diseases, X-Linked [MESH:D040181] (3028)   Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Mental Retardation, X-Linked [MESH:D038901] (1867)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Mental Retardation, X-Linked 30 [MESH:C563146] (40)  Mental Retardation, X-Linked, with Epilepsy [MESH:C564516] (34)  Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Coffin-Lowry Syndrome [MESH:D038921] (45)  Fragile X Syndrome [MESH:D005600] (353)  Hemoglobinopathies [MESH:D006453] (1863)   Anemia, Sickle Cell [MESH:D000755] (1722)  Thalassemia [MESH:D013789] (511)   alpha-Thalassemia [MESH:D017085] (192)  beta-Thalassemia [MESH:D017086] (458)  Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)   Familial encephalopathy with neuroserpin inclusion bodies [MESH:C536841] (40)  Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Alexander Disease [MESH:D038261] (168)  Gerstmann-Straussler-Scheinker Disease [MESH:D016098] (98)  Hepatolenticular Degeneration [MESH:D006527] (473)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (241)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Hereditary Sensory and Motor Neuropathy [MESH:D015417] (899)   Charcot-Marie-Tooth Disease [MESH:D002607] (627)   Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219)  Charcot-Marie-Tooth Disease, Axonal, Type 2a1 [MESH:C566138] (54)  Spastic Paraplegia, Hereditary [MESH:D015419] (449)   Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178)  Huntington Disease [MESH:D006816] (540)   Huntington Disease-Like 1 [MESH:C566398] (98)  Mental Retardation, X-Linked [MESH:D038901] (1848)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Mental Retardation, X-Linked 30 [MESH:C563146] (40)  Mental Retardation, X-Linked, with Epilepsy [MESH:C564516] (34)  Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia [MESH:C567466] (28)  Coffin-Lowry Syndrome [MESH:D038921] (45)  Fragile X Syndrome [MESH:D005600] (353)  Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 2 [MESH:C566857] (39)  Spinocerebellar Degenerations [MESH:D013132] (449)   Spinocerebellar Ataxia 29 [MESH:C537206] (90)  Spinocerebellar Ataxias [MESH:D020754] (322)   Spinocerebellar Ataxia 15 [MESH:C564685] (90)  Metabolism, Inborn Errors [MESH:D008661] (6032)   Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)   Glutamine deficiency, congenital [MESH:C536832] (117)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Alexander Disease [MESH:D038261] (168)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease of Heart, Lethal Congenital [MESH:C564888] (30)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 2 [MESH:C566857] (39)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Congenital atransferrinemia [MESH:C538259] (145)  Hepatolenticular Degeneration [MESH:D006527] (473)  Muscular Dystrophies [MESH:D009136] (1597)   Distal Myopathies [MESH:D049310] (178)  Myasthenic Syndromes, Congenital [MESH:D020294] (155)   Myopathy, Congenital, Compton-North [MESH:C567261] (35)  Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)   Exostoses, Multiple Hereditary [MESH:D005097] (154)   Metachondromatosis [MESH:C562938] (49)  Skin Diseases, Genetic [MESH:D012873] (3456)   Buschke-Ollendorff syndrome [MESH:C537415] (11)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Infant, Newborn, Diseases [MESH:D007232] (3064)   Epilepsy, Benign Neonatal [MESH:D020936] (57) C17. Skin and Connective Tissue Diseases  C17. Skin and Connective Tissue Diseases  Connective Tissue Diseases [MESH:D003240] (4490)   Dermatomyositis [MESH:D003882] (1826)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Collagen Diseases [MESH:D003095] (1267)   Keloid [MESH:D007627] (1111)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Noonan Syndrome [MESH:D009634] (506)   Noonan syndrome 3 [MESH:C537847] (118)  Osteopoikilosis [MESH:D010023] (15)   Buschke-Ollendorff syndrome [MESH:C537415] (11)  Panniculitis [MESH:D015434] (91)   Panniculitis, Nodular Nonsuppurative [MESH:D010201] (78)  Rheumatic Diseases [MESH:D012216] (3619)   Arthritis, Rheumatoid [MESH:D001172] (3603)  Skin Diseases [MESH:D012871] (8774)   Dermatomyositis [MESH:D003882] (1826)  Exanthema [MESH:D005076] (301)  Pruritus [MESH:D011537] (647)  Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Breast Diseases [MESH:D001941] (6148)   Breast Neoplasms [MESH:D001943] (6077)  Dermatitis [MESH:D003872] (4530)   Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Erythema [MESH:D004890] (1330)   Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Facial Dermatoses [MESH:D005148] (1336)   Acneiform Eruptions [MESH:D017486] (1312)   Chloracne [MESH:D054506] (1274)  Panniculitis [MESH:D015434] (88)   Panniculitis, Nodular Nonsuppurative [MESH:D010201] (78)  Pigmentation Disorders [MESH:D010859] (1215)   Hyperpigmentation [MESH:D017495] (523)   Melanosis [MESH:D008548] (459)   Lentigo [MESH:D007911] (329)   LEOPARD Syndrome [MESH:D044542] (299)  Skin Abnormalities [MESH:D012868] (1709)   Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Skin Diseases, Genetic [MESH:D012873] (3481)   Buschke-Ollendorff syndrome [MESH:C537415] (11)  Ectodermal Dysplasia [MESH:D004476] (958)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Ehlers-Danlos Syndrome [MESH:D004535] (491)   Ehlers-Danlos syndrome type 1 [MESH:C536194] (344)  Skin Diseases, Papulosquamous [MESH:D017444] (3392)   Parapsoriasis [MESH:D010267] (49)  Psoriasis [MESH:D011565] (3278)   Arthritis, Psoriatic [MESH:D015535] (1859)  Skin Diseases, Vascular [MESH:D017445] (3288)   Behcet Syndrome [MESH:D001528] (1784)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Skin Diseases, Vesiculobullous [MESH:D012872] (1754)   Pemphigus [MESH:D010392] (158)  Erythema Multiforme [MESH:D004892] (1185)   Stevens-Johnson Syndrome [MESH:D013262] (1163) C18. Nutritional and Metabolic Diseases  C18. Nutritional and Metabolic Diseases  Metabolic Diseases [MESH:D008659] (9025)   Brain Diseases, Metabolic [MESH:D001928] (3350)   Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Alexander Disease [MESH:D038261] (168)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Calcium Metabolism Disorders [MESH:D002128] (3634)   Calcinosis [MESH:D002114] (2989)  Glucose Metabolism Disorders [MESH:D044882] (6122)   Hyperglycemia [MESH:D006943] (1858)  Diabetes Mellitus [MESH:D003920] (5891)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Hyperinsulinism [MESH:D006946] (3586)   Hyperinsulinemic hypoglycemia, familial, 6 [MESH:C538375] (64)  Insulin Resistance [MESH:D007333] (3511)  Hypoglycemia [MESH:D007003] (2420)   Hyperinsulinemic hypoglycemia, familial, 6 [MESH:C538375] (64)  Iron Metabolism Disorders [MESH:D019189] (2139)   Iron Overload [MESH:D019190] (1772)  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)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 2 [MESH:C566857] (39)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Metabolism, Inborn Errors [MESH:D008661] (6028)   Hypoproteinemia, Hypercatabolic [MESH:C565476] (99)  Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)  Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)   Glutamine deficiency, congenital [MESH:C536832] (117)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)   Hepatolenticular Degeneration [MESH:D006527] (473)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)   Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Alexander Disease [MESH:D038261] (168)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)   Glycogen Storage Disease [MESH:D006008] (530)   Glycogen Storage Disease of Heart, Lethal Congenital [MESH:C564888] (30)  Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)   Hyperlipoproteinemia Type II [MESH:D006938] (707)  Hyperlipoproteinemia Type III [MESH:D006952] (181)  Lipidoses [MESH:D008064] (1655)   Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)   Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946)  Ceroid Lipofuscinosis, Neuronal, 2 [MESH:C566857] (39)  Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Lysosomal Storage Diseases [MESH:D016464] (761)   Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)   Sphingolipidoses [MESH:D013106] (582)   Sea-Blue Histiocyte Syndrome [MESH:D012618] (165)  Gaucher Disease [MESH:D005776] (299)   Gaucher Disease, Atypical, Due To Saposin C Deficiency [MESH:C566435] (56)  Leukodystrophy, Globoid Cell [MESH:D007965] (65)   Krabbe Disease, Atypical, due to Saposin A Deficiency [MESH:C567097] (56)  Sulfatidosis [MESH:D052516] (86)   Leukodystrophy, Metachromatic [MESH:D007966] (76)   Metachromatic Leukodystrophy due to Saposin B Deficiency [MESH:C562609] (56)  Combined Saposin Deficiency [MESH:C567125] (56)  Metal Metabolism, Inborn Errors [MESH:D008664] (2017)   Congenital atransferrinemia [MESH:C538259] (145)  Hepatolenticular Degeneration [MESH:D006527] (473)  Mitochondrial Diseases [MESH:D028361] (2561)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178)  Mitochondrial Myopathies [MESH:D017240] (2176)   Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1313)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Proteostasis Deficiencies [MESH:D057165] (3522)   Amyloidosis [MESH:D000686] (791)   Amyloid Neuropathies [MESH:D017772] (139)   Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Amyloidosis, Familial [MESH:D028226] (696)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Amyloid Neuropathies, Familial [MESH:D028227] (137)   Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)  Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  Cerebral Amyloid Angiopathy [MESH:D016657] (470)   Cerebral Amyloid Angiopathy, Familial [MESH:D028243] (377)   Cerebral Amyloid Angiopathy, App-Related [MESH:C567787] (333)  TDP-43 Proteinopathies [MESH:D057177] (3337)   Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)   Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)  Water-Electrolyte Imbalance [MESH:D014883] (2790)   Hyponatremia [MESH:D007010] (789)  Water Intoxication [MESH:D014869] (106)  Nutrition Disorders [MESH:D009748] (4945)   Malnutrition [MESH:D044342] (2754)   Deficiency Diseases [MESH:D003677] (2742)   Avitaminosis [MESH:D001361] (2304)   Vitamin B Deficiency [MESH:D014804] (1817)   Thiamine Deficiency [MESH:D013832] (139)  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 Cortex Diseases [MESH:D000303] (969)   Pigmented Nodular Adrenocortical Disease, Primary, 1 [MESH:C566469] (34)  Diabetes Mellitus [MESH:D003920] (6159)   Diabetes Mellitus, Experimental [MESH:D003921] (4771)  Diabetes Mellitus, Type 1 [MESH:D003922] (1897)  Diabetes Mellitus, Type 2 [MESH:D003924] (4219)  Diabetes Complications [MESH:D048909] (4129)   Diabetic Cardiomyopathies [MESH:D058065] (1995)  Diabetic Nephropathies [MESH:D003928] (2301)  Diabetic Angiopathies [MESH:D003925] (1984)   Diabetic Retinopathy [MESH:D003930] (1371)  Endocrine Gland Neoplasms [MESH:D004701] (4925)   Ovarian Neoplasms [MESH:D010051] (3275)  Pancreatic Neoplasms [MESH:D010190] (3820)   Carcinoma, Pancreatic Ductal [MESH:D021441] (1056)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111)  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)   Cryptorchidism [MESH:D003456] (215)   Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Thyroid Diseases [MESH:D013959] (2808)   Goiter [MESH:D006042] (359)   Graves Disease [MESH:D006111] (278)  Hyperthyroidism [MESH:D006980] (1191)   Graves Disease [MESH:D006111] (278)  Hyperthyroxinemia [MESH:D006981] (659)   Dystransthyretinemic Euthyroidal Hyperthyroxinemia [MESH:C567719] (136)  Thyroid Neoplasms [MESH:D013964] (2040)   Thyroid cancer, papillary [MESH:C536915] (111) C20. Immune System Diseases  C20. Immune System Diseases  Immune System Diseases [MESH:D007154] (7674)   Autoimmune Diseases [MESH:D001327] (5067)   Arthritis, Rheumatoid [MESH:D001172] (3601)  Diabetes Mellitus, Type 1 [MESH:D003922] (1893)  Glomerulonephritis, Membranous [MESH:D015433] (642)  Graves Disease [MESH:D006111] (278)  Lupus Erythematosus, Systemic [MESH:D008180] (2317)  Pemphigus [MESH:D010392] (158)  Autoimmune Diseases of the Nervous System [MESH:D020274] (2238)   Myasthenia Gravis [MESH:D009157] (632)  Demyelinating Autoimmune Diseases, CNS [MESH:D020278] (1732)   Neuromyelitis Optica [MESH:D009471] (248)  Multiple Sclerosis [MESH:D009103] (1716)   Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170)  Neuromyelitis Optica [MESH:D009471] (248)  Myelitis, Transverse [MESH:D009188] (255)   Neuromyelitis Optica [MESH:D009471] (248)  Hypersensitivity [MESH:D006967] (5873)   Drug Hypersensitivity [MESH:D004342] (4000)   Drug Eruptions [MESH:D003875] (2695)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Hypersensitivity, Immediate [MESH:D006969] (4980)   Respiratory Hypersensitivity [MESH:D012130] (4250)   Asthma [MESH:D001249] (3914)  Urticaria [MESH:D014581] (2668)   Angioedema [MESH:D000799] (837)  Immune Complex Diseases [MESH:D007105] (782)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Immunologic Deficiency Syndromes [MESH:D007153] (3788)   HIV Infections [MESH:D015658] (3402)  Phagocyte Bactericidal Dysfunction [MESH:D010585] (999)   Job Syndrome [MESH:D007589] (772)   Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283)  Immunoproliferative Disorders [MESH:D007160] (4761)   Hypergammaglobulinemia [MESH:D006942] (137)  Lymphoproliferative Disorders [MESH:D008232] (4734)   Multiple Myeloma [MESH:D009101] (2767)  Leukemia, Lymphoid [MESH:D007945] (3047)   Leukemia, T-Cell [MESH:D015458] (395)  Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)   Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354)  Lymphoma [MESH:D008223] (3684)   Lymphoma, Non-Hodgkin [MESH:D008228] (3330)   Lymphoma, B-Cell [MESH:D016393] (2624)   Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)  Lymphoma, T-Cell [MESH:D016399] (1382)   Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420)  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)  Paratuberculosis [MESH:D010283] (427)  Sheep Diseases [MESH:D012757] (473)   Scrapie [MESH:D012608] (462) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Pathological Conditions, Anatomical [MESH:D020763] (6074)   Atrophy [MESH:D001284] (2603)  Plaque, Amyloid [MESH:D058225] (334)  Plaque, Atherosclerotic [MESH:D058226] (696)  Agenesis of Corpus Callosum [MESH:D061085] (197)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Calculi [MESH:D002137] (756)   Urinary Calculi [MESH:D014545] (521)   Kidney Calculi [MESH:D007669] (455)  Cysts [MESH:D003560] (133)   Leukoencephalopathy, Cystic, Without Megalencephaly [MESH:C567845] (25)  Hernia [MESH:D006547] (2825)   Hernia, Diaphragmatic [MESH:D006548] (2647)  Intervertebral Disc Displacement [MESH:D007405] (520)   Intervertebral disc disease [MESH:C535531] (514)  Hypertrophy [MESH:D006984] (4476)   Cardiomegaly [MESH:D006332] (3802)  Splenomegaly [MESH:D013163] (1258)  Polyps [MESH:D011127] (1633)   Intestinal Polyps [MESH:D007417] (1592)  Pathologic Processes [MESH:D010335] (9863)   Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Gliosis [MESH:D005911] (1419)  Hyperammonemia [MESH:D022124] (322)  Hyperplasia [MESH:D006965] (2463)  Ischemia [MESH:D007511] (3049)  Necrosis [MESH:D009336] (4019)  Nerve Degeneration [MESH:D009410] (4061)  Arrhythmias, Cardiac [MESH:D001145] (4658)   Cardiac Arrhythmia, Ankyrin-B-Related [MESH:C566996] (32)  Bradycardia [MESH:D001919] (1899)  Death [MESH:D003643] (1328)   Embryo Loss [MESH:D020964] (288)  Fetal Death [MESH:D005313] (464)  Death, Sudden [MESH:D003645] (725)   Sudden Infant Death [MESH:D013398] (268)  Disease Attributes [MESH:D020969] (3654)   Disease Progression [MESH:D018450] (2868)  Disease Susceptibility [MESH:D004198] (1200)   Genetic Predisposition to Disease [MESH:D020022] (966)  Facies [MESH:D019066] (738)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Emphysema [MESH:D004646] (1096)   Subcutaneous Emphysema [MESH:D013352] (82)   alpha 1-Antitrypsin Deficiency [MESH:D019896] (80)  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)  Growth Disorders [MESH:D006130] (2438)   Fetal Growth Retardation [MESH:D005317] (986)   Bowen-Conradi syndrome [MESH:C537081] (18)  Hemorrhage [MESH:D006470] (4451)   Intracranial Hemorrhages [MESH:D020300] (3241)   Cerebral Hemorrhage [MESH:D002543] (2872)   Cerebral hemorrhage with amyloidosis, hereditary, Dutch type [MESH:C537944] (333)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Inflammation [MESH:D007249] (5241)   Neurogenic Inflammation [MESH:D020078] (2246)  Systemic Inflammatory Response Syndrome [MESH:D018746] (3563)   Sepsis [MESH:D018805] (3562)   Bacteremia [MESH:D016470] (1369)   Endotoxemia [MESH:D019446] (1289)  Menstruation Disturbances [MESH:D008599] (926)   Dysmenorrhea [MESH:D004412] (189)  Metaplasia [MESH:D008679] (1469)   Neovascularization, Pathologic [MESH:D009389] (829)  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)  Postoperative Complications [MESH:D011183] (5311)   Reperfusion Injury [MESH:D015427] (4968)   Myocardial Reperfusion Injury [MESH:D015428] (3500)  Signs and Symptoms [MESH:D012816] (10659)   Cyanosis [MESH:D003490] (288)  Edema [MESH:D004487] (3726)  Fetal Distress [MESH:D005316] (99)  Flushing [MESH:D005483] (506)  Hypergammaglobulinemia [MESH:D006942] (105)  Body Weight [MESH:D001835] (4972)   Body Weight Changes [MESH:D001836] (3206)   Weight Gain [MESH:D015430] (2595)  Weight Loss [MESH:D015431] (2512)  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)  Tremor [MESH:D014202] (840)  Neurobehavioral Manifestations [MESH:D019954] (4706)   Communication Disorders [MESH:D003147] (2918)   Learning Disorders [MESH:D007859] (2727)  Language Disorders [MESH:D007806] (653)   Language Development Disorders [MESH:D007805] (351)  Speech Disorders [MESH:D013064] (482)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Stuttering [MESH:D013342] (38)  Consciousness Disorders [MESH:D003244] (677)   Unconsciousness [MESH:D014474] (657)   Coma [MESH:D003128] (492)  Memory Disorders [MESH:D008569] (3233)   Amnesia [MESH:D000647] (1911)  Intellectual Disability [MESH:D008607] (1476)   Coffin-Siris syndrome [MESH:C536436] (102)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Psychomotor Disorders [MESH:D011596] (576)   Bowen-Conradi syndrome [MESH:C537081] (18)  Neuromuscular Manifestations [MESH:D020879] (2130)   Muscle Hypertonia [MESH:D009122] (775)  Spasm [MESH:D013035] (418)  Muscle Hypotonia [MESH:D009123] (258)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Pain [MESH:D010146] (3869)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 [MESH:C563575] (77)  Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311)   Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 [MESH:C563750] (56)  Reflex, Abnormal [MESH:D012021] (485)   Reflex, Babinski [MESH:D001405] (97)  Sensation Disorders [MESH:D012678] (5009)   Taste Disorders [MESH:D013651] (461)  Hearing Disorders [MESH:D006311] (2101)   Hearing Loss [MESH:D034381] (2066)   Hearing Loss, Sensorineural [MESH:D006319] (1227)  Somatosensory Disorders [MESH:D020886] (4000)   Hyperalgesia [MESH:D006930] (3929)  Pain [MESH:D010146] (4511)   Headache [MESH:D006261] (1417)  Neuralgia [MESH:D009437] (2074)  Chest Pain [MESH:D002637] (2642)   Angina Pectoris [MESH:D000787] (2568)   Acute Coronary Syndrome [MESH:D054058] (2286)  Pelvic Pain [MESH:D017699] (198)   Dysmenorrhea [MESH:D004412] (189)  Signs and Symptoms, Digestive [MESH:D012817] (3095)   Hyperphagia [MESH:D006963] (206)  Constipation [MESH:D003248] (506)   Opitz-Kaveggia syndrome [MESH:C537923] (64)  Signs and Symptoms, Respiratory [MESH:D012818] (2724)   Anoxia [MESH:D000860] (1698)  Hyperventilation [MESH:D006985] (652)   Pitt-Hopkins syndrome [MESH:C537403] (113)  Skin Manifestations [MESH:D012877] (1250)   Pruritus [MESH:D011537] (648)  Purpura [MESH:D011693] (475)   Purpura, Schoenlein-Henoch [MESH:D011695] (266)  Urological Manifestations [MESH:D020924] (3532)   Polyuria [MESH:D011141] (279)  Proteinuria [MESH:D011507] (3293)   Hemoglobinuria [MESH:D006456] (75)   CD59 Deficiency [MESH:C567355] (57) C24. Occupational Diseases  C24. Occupational Diseases  Occupational Diseases [MESH:D009784] (3402)   Pneumoconiosis [MESH:D011009] (2670)   Asbestosis [MESH:D001195] (935)  Berylliosis [MESH:D001607] (2005)  Sleep Disorders, Circadian Rhythm [MESH:D020178] (93)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82) C25. Chemically-Induced Disorders  C25. Chemically-Induced Disorders  Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)   Drug-Induced Liver Injury [MESH:D056486] (4936)  Drug Hypersensitivity [MESH:D004342] (4001)   Drug Eruptions [MESH:D003875] (2697)   Stevens-Johnson Syndrome [MESH:D013262] (1163)  Poisoning [MESH:D011041] (6703)   Arsenic Poisoning [MESH:D020261] (2540)  Cadmium Poisoning [MESH:D002105] (180)  Drug-Induced Liver Injury [MESH:D056486] (4936)  Manganese Poisoning [MESH:D020149] (2214)  Mercury Poisoning [MESH:D008630] (193)  Psychoses, Substance-Induced [MESH:D011605] (2053)  Water Intoxication [MESH:D014869] (106)  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)  Psychoses, Substance-Induced [MESH:D011605] (2052)  Substance Withdrawal Syndrome [MESH:D013375] (2956)  Alcohol-Related Disorders [MESH:D019973] (3869)   Alcoholic Intoxication [MESH:D000435] (87)  Alcoholism [MESH:D000437] (1519)  Alcohol-Induced Disorders [MESH:D020751] (3350)   Liver Diseases, Alcoholic [MESH:D008108] (3243) C26. Wounds and Injuries  C26. Wounds and Injuries  Z. Exceptions (2454)   Not Fully Specified [NFS] (2454)  Wounds and Injuries [MESH:D014947] (5171)   Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506)  Vascular System Injuries [MESH:D057772] (2086)  Craniocerebral Trauma [MESH:D006259] (3523)   Brain Injuries [MESH:D001930] (3431)  Sprains and Strains [MESH:D013180] (153)   Cumulative Trauma Disorders [MESH:D012090] (151)   Carpal Tunnel Syndrome [MESH:D002349] (147)  Trauma, Nervous System [MESH:D020196] (3535)   Craniocerebral Trauma [MESH:D006259] (3507)   Brain Injuries [MESH:D001930] (3431) D02. Organic Chemicals  D02. Organic Chemicals  Organic Chemicals [MESH:D009930] (75987)   Hydrocarbons [MESH:D006838] (35762)   Hydrocarbons, Cyclic [MESH:D006844] (22983)   Hydrocarbons, Alicyclic [MESH:D006840] (3199)   Cycloparaffins [MESH:D003516] (3197)   Cycloheptanes [MESH:D003508] (224)   Tropolone [MESH:D014334] (47) E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  E. Analytical, Diagnostic and Therapeutic Techniques and Equipment  Diagnosis [MESH:D003933] (1924)   Diagnostic Techniques and Procedures [MESH:D019937] (1902)   Physical Examination [MESH:D010808] (1041)   Facies [MESH:D019066] (704)   Cardiofaciocutaneous syndrome [MESH:C535579] (407)  Pitt-Hopkins syndrome [MESH:C537403] (113) 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)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Psychomotor Disorders [MESH:D011596] (250)   Bowen-Conradi syndrome [MESH:C537081] (18)  Mental Disorders [MESH:D001523] (2063)   Spongiform Encephalopathy with Neuropsychiatric Features [MESH:C564678] (98)  Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)   Cognition Disorders [MESH:D003072] (115)   Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Dementia [MESH:D003704] (471)   Alzheimer Disease [MESH:D000544] (242)   Alzheimer disease type 2 [MESH:C536595] (165)  Huntington Disease [MESH:D006816] (102)   Huntington Disease-Like 1 [MESH:C566398] (98)  Lewy Body Disease [MESH:D020961] (139)   Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136)  Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)   Developmental Disabilities [MESH:D002658] (151)   Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Intellectual Disability [MESH:D008607] (1109)   Coffin-Siris syndrome [MESH:C536436] (102)  Pitt-Hopkins syndrome [MESH:C537403] (113)  Cleft Palate, Isolated, And Mental Retardation [MESH:C566991] (65)  Arginine:Glycine Amidinotransferase Deficiency [MESH:C567192] (66)  Skeletal Defects, Genital Hypoplasia, And Mental Retardation [MESH:C567306] (52)  Sleep Disorders [MESH:D012893] (148)   Dyssomnias [MESH:D020920] (101)   Sleep Disorders, Circadian Rhythm [MESH:D020178] (84)   Advanced Sleep-Phase Syndrome, Familial [MESH:C565789] (82)