Select any link to see items in a related category.

more general categories	information about this item
A. Anatomy	A. Anatomy
Musculoskeletal System [MESH:D009141] (1255)
Skeleton [MESH:D012863] (1177)
Bone and Bones [MESH:D001842] (1112)
Epiphyses [MESH:D004838] (98)	Wolcott-Rallison syndrome [MESH:C536739] (92)
C01. Bacterial Infections and Mycoses	C01. Bacterial Infections and Mycoses
Bacterial Infections [MESH:D001424] (3716)
Gram-Negative Bacterial Infections [MESH:D016905] (3085)	Helicobacter Infections [MESH:D016481] (579)
Gram-Positive Bacterial Infections [MESH:D016908] (2434)
Actinomycetales Infections [MESH:D000193] (1466)
Mycobacterium Infections [MESH:D009164] (1446)	Mycobacterium Infections, Nontuberculous [MESH:D009165] (480)
Tuberculosis [MESH:D014376] (992)	Tuberculosis, Pulmonary [MESH:D014397] (678)
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)
Central Nervous System Viral Diseases [MESH:D020805] (1416)
Meningitis, Viral [MESH:D008587] (1308)	Meningitis, Aseptic [MESH:D008582] (1305)
DNA Virus Infections [MESH:D004266] (2474)
Hepadnaviridae Infections [MESH:D018347] (977)	Hepatitis B [MESH:D006509] (976)
Herpesviridae Infections [MESH:D006566] (1944)	Sarcoma, Kaposi [MESH:D012514] (1578)
Epstein-Barr Virus Infections [MESH:D020031] (695)	Burkitt Lymphoma [MESH:D002051] (691)
Hepatitis, Viral, Human [MESH:D006525] (1766)	Hepatitis B [MESH:D006509] (976)
Meningitis, Viral [MESH:D008587] (1308)	Meningitis, Aseptic [MESH:D008582] (1305)
RNA Virus Infections [MESH:D012327] (4215)
Orthomyxoviridae Infections [MESH:D009976] (1077)	Influenza, Human [MESH:D007251] (1075)
Retroviridae Infections [MESH:D012192] (3420)
Lentivirus Infections [MESH:D016180] (3408)
HIV Infections [MESH:D015658] (3402)	HIV Wasting Syndrome [MESH:D019247] (1956)
Sexually Transmitted Diseases [MESH:D012749] (3305)
Sexually Transmitted Diseases, Viral [MESH:D015229] (3304)
HIV Infections [MESH:D015658] (3296)	HIV Wasting Syndrome [MESH:D019247] (1956)
Tumor Virus Infections [MESH:D014412] (1069)
Epstein-Barr Virus Infections [MESH:D020031] (693)	Burkitt Lymphoma [MESH:D002051] (691)
C03. Parasitic Diseases	C03. Parasitic Diseases
Parasitic Diseases [MESH:D010272] (3828)
Helminthiasis [MESH:D006373] (1644)
Trematode Infections [MESH:D014201] (1182)	Schistosomiasis [MESH:D012552] (1073)
Protozoan Infections [MESH:D011528] (3014)	Malaria [MESH:D008288] (2175)
Amebiasis [MESH:D000562] (1711)	Entamoebiasis [MESH:D004749] (1689)
Euglenozoa Infections [MESH:D056986] (2552)
Leishmaniasis [MESH:D007896] (2541)	Leishmaniasis, Cutaneous [MESH:D016773] (2359)
	Leishmaniasis, Visceral [MESH:D007898] (2149)
Skin Diseases, Parasitic [MESH:D012876] (2541)
Leishmaniasis [MESH:D007896] (2516)	Leishmaniasis, Cutaneous [MESH:D016773] (2359)
C04. Neoplasms	C04. Neoplasms
Neoplasms [MESH:D009369] (10293)
Neoplasms by Histologic Type [MESH:D009370] (8793)
Leukemia [MESH:D007938] (4576)
Leukemia, Lymphoid [MESH:D007945] (3047)	Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)
Leukemia, B-Cell [MESH:D015448] (2564)	Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
Leukemia, Myeloid [MESH:D007951] (2773)	Leukemia, Myeloid, Acute [MESH:D015470] (2176)
	Leukemia, Myelomonocytic, Acute [MESH:D015479] (85)
Lymphoma [MESH:D008223] (3686)
Lymphoma, Non-Hodgkin [MESH:D008228] (3337)	Burkitt Lymphoma [MESH:D002051] (691)
Lymphoma, B-Cell [MESH:D016393] (2624)	Burkitt Lymphoma [MESH:D002051] (691)
	Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
Neoplasms, Connective and Soft Tissue [MESH:D018204] (4742)	Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)
Neoplasms, Connective Tissue [MESH:D009372] (3626)	Chondroma [MESH:D002812] (155)
Chondrosarcoma [MESH:D002813] (1217)	Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)
Neoplasms, Bone Tissue [MESH:D018213] (2217)	Osteosarcoma [MESH:D012516] (2175)
Neoplasms, Muscle Tissue [MESH:D009379] (1965)	Leiomyosarcoma [MESH:D007890] (977)
Sarcoma [MESH:D012509] (4246)	Hemangiosarcoma [MESH:D006394] (1836)
	Leiomyosarcoma [MESH:D007890] (977)
	Osteosarcoma [MESH:D012516] (2175)
	Sarcoma, Kaposi [MESH:D012514] (1578)
Chondrosarcoma [MESH:D002813] (1217)	Chondrosarcoma, Extraskeletal Myxoid [MESH:C563195] (98)
Neoplasms, Germ Cell and Embryonal [MESH:D009373] (5126)
Neuroectodermal Tumors [MESH:D017599] (5066)
Neoplasms, Neuroepithelial [MESH:D018302] (4487)
Glioma [MESH:D005910] (4261)	Gliosarcoma [MESH:D018316] (880)
	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)
Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)
Adenoma [MESH:D000236] (4051)	Mesothelioma [MESH:D008654] (2567)
Adenomatous Polyps [MESH:D018256] (1571)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Carcinoma [MESH:D002277] (7263)	Carcinoma, Basal Cell [MESH:D002280] (1628)
	Carcinoma in Situ [MESH:D002278] (2111)
	Carcinoma, Transitional Cell [MESH:D002295] (2662)
Adenocarcinoma [MESH:D000230] (6565)	Adenocarcinoma of lung [MESH:C538231] (1487)
	Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
	Carcinoma, Hepatocellular [MESH:D006528] (5375)
	Carcinoma, Renal Cell [MESH:D002292] (2975)
	Cholangiocarcinoma [MESH:D018281] (2398)
Carcinoma, Ductal [MESH:D044584] (1786)	Carcinoma, Ductal, Breast [MESH:D018270] (1112)
Carcinoma, Squamous Cell [MESH:D002294] (4294)	Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
	Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
Neoplasms, Basal Cell [MESH:D018295] (1707)	Carcinoma, Basal Cell [MESH:D002280] (1628)
Neoplasms, Ductal, Lobular, and Medullary [MESH:D018299] (1831)
Carcinoma, Ductal [MESH:D044584] (1786)	Carcinoma, Ductal, Breast [MESH:D018270] (1112)
Neoplasms, Mesothelial [MESH:D018301] (2569)	Mesothelioma [MESH:D008654] (2567)
Neoplasms, Neuroepithelial [MESH:D018302] (4487)
Glioma [MESH:D005910] (4261)	Gliosarcoma [MESH:D018316] (880)
	Medulloblastoma [MESH:D008527] (1282)
	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)	Papilloma [MESH:D010212] (2243)
Carcinoma, Squamous Cell [MESH:D002294] (4294)	Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
	Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
Neoplasms, Nerve Tissue [MESH:D009380] (5201)
Neuroectodermal Tumors [MESH:D017599] (5059)
Neoplasms, Neuroepithelial [MESH:D018302] (4487)
Glioma [MESH:D005910] (4261)	Gliosarcoma [MESH:D018316] (880)
	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)
Neoplasms, Plasma Cell [MESH:D054219] (2772)	Multiple Myeloma [MESH:D009101] (2767)
Neoplasms, Vascular Tissue [MESH:D009383] (2959)	Hemangiosarcoma [MESH:D006394] (1836)
	Sarcoma, Kaposi [MESH:D012514] (1578)
Hemangioma [MESH:D006391] (690)
Hemangioma, Capillary [MESH:D018324] (503)	Hemangioma, capillary infantile [MESH:C535860] (190)
Nevi and Melanomas [MESH:D018326] (3572)	Melanoma [MESH:D008545] (3508)
Neoplasms by Site [MESH:D009371] (9169)	Bone Neoplasms [MESH:D001859] (1334)
	Skin Neoplasms [MESH:D012878] (2992)
Breast Neoplasms [MESH:D001943] (6077)	Carcinoma, Ductal, Breast [MESH:D018270] (1112)
Digestive System Neoplasms [MESH:D004067] (7487)	Pancreatic Neoplasms [MESH:D010190] (3820)
Gastrointestinal Neoplasms [MESH:D005770] (6452)	Stomach Neoplasms [MESH:D013274] (4942)
Esophageal Neoplasms [MESH:D004938] (3737)	Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
	Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
Intestinal Neoplasms [MESH:D007414] (5358)
Colorectal Neoplasms [MESH:D015179] (5294)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Colonic Neoplasms [MESH:D003110] (4405)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Liver Neoplasms [MESH:D008113] (6048)	Carcinoma, Hepatocellular [MESH:D006528] (5375)
	Liver Neoplasms, Experimental [MESH:D008114] (2837)
Endocrine Gland Neoplasms [MESH:D004701] (4925)	Ovarian Neoplasms [MESH:D010051] (3275)
	Pancreatic Neoplasms [MESH:D010190] (3820)
	Thyroid Neoplasms [MESH:D013964] (2040)
Head and Neck Neoplasms [MESH:D006258] (4612)	Carcinoma, squamous cell of head and neck [MESH:C535575] (1543)
	Thyroid Neoplasms [MESH:D013964] (2040)
Esophageal Neoplasms [MESH:D004938] (3737)	Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
	Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
Mouth Neoplasms [MESH:D009062] (2263)	Leukoplakia, Oral [MESH:D007972] (921)
	Tongue Neoplasms [MESH:D014062] (1518)
Mammary Neoplasms, Animal [MESH:D015674] (3404)	Mammary Neoplasms, Experimental [MESH:D008325] (3268)
Thoracic Neoplasms [MESH:D013899] (6032)
Respiratory Tract Neoplasms [MESH:D012142] (6020)
Lung Neoplasms [MESH:D008175] (6015)	Adenocarcinoma of lung [MESH:C538231] (1487)
Bronchial Neoplasms [MESH:D001984] (3608)
Carcinoma, Bronchogenic [MESH:D002283] (3606)	Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540)
Urogenital Neoplasms [MESH:D014565] (7002)
Genital Neoplasms, Female [MESH:D005833] (2540)
Uterine Neoplasms [MESH:D014594] (2431)	Endometrial Neoplasms [MESH:D016889] (1987)
Genital Neoplasms, Male [MESH:D005834] (6224)	Prostatic Neoplasms [MESH:D011471] (6135)
Urologic Neoplasms [MESH:D014571] (5315)	Urinary Bladder Neoplasms [MESH:D001749] (4079)
Kidney Neoplasms [MESH:D007680] (3966)	Carcinoma, Renal Cell [MESH:D002292] (2975)
Neoplasms, Experimental [MESH:D009374] (5218)	Liver Neoplasms, Experimental [MESH:D008114] (2837)
	Mammary Neoplasms, Experimental [MESH:D008325] (3268)
Tumor Virus Infections [MESH:D014412] (697)
Epstein-Barr Virus Infections [MESH:D020031] (693)	Burkitt Lymphoma [MESH:D002051] (691)
Neoplastic Processes [MESH:D009385] (5317)	Neoplasm Invasiveness [MESH:D009361] (3388)
	Neoplasm 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)	Hemangioma, capillary infantile [MESH:C535860] (190)
	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Precancerous Conditions [MESH:D011230] (2858)
Leukoplakia [MESH:D007971] (922)	Leukoplakia, Oral [MESH:D007972] (921)
Tumor Virus Infections [MESH:D014412] (759)
Epstein-Barr Virus Infections [MESH:D020031] (693)	Burkitt Lymphoma [MESH:D002051] (691)
C05. Musculoskeletal Diseases	C05. Musculoskeletal Diseases
Musculoskeletal Diseases [MESH:D009140] (8705)
Bone Diseases [MESH:D001847] (5801)	Bone Neoplasms [MESH:D001859] (1334)
	Bone Resorption [MESH:D001862] (2352)
Bone Diseases, Developmental [MESH:D001848] (3315)
Dysostoses [MESH:D004413] (1019)
Synostosis [MESH:D013580] (817)	Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)
Osteochondrodysplasias [MESH:D010009] (2440)	Spondyloenchondrodysplasia [MESH:C535782] (71)
	Wolcott-Rallison syndrome [MESH:C536739] (92)
	Enchondromatosis [MESH:D004687] (170)
	Pycnodysostosis [MESH:D058631] (73)
Chondrodysplasia Punctata [MESH:D002806] (108)	Chondrodysplasia punctata 2, X-linked dominant [MESH:C538416] (61)
Bone Diseases, Metabolic [MESH:D001851] (3492)
Osteoporosis [MESH:D010024] (3037)	Osteoporosis, Postmenopausal [MESH:D015663] (2351)
Osteitis Deformans [MESH:D010001] (287)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Jaw Diseases [MESH:D007571] (1601)
Jaw Abnormalities [MESH:D007569] (1435)	Cleft Palate [MESH:D002972] (1330)
Joint Diseases [MESH:D007592] (4657)
Arthritis [MESH:D001168] (4416)	Arthritis, Experimental [MESH:D001169] (3142)
	Arthritis, Juvenile [MESH:D001171] (1060)
	Arthritis, Rheumatoid [MESH:D001172] (3603)
	Osteoarthritis [MESH:D010003] (1743)
Arthrogryposis [MESH:D001176] (329)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
Muscular Diseases [MESH:D009135] (4071)	VLCAD deficiency [MESH:C536353] (55)
	Muscle Rigidity [MESH:D009127] (617)
Arthrogryposis [MESH:D001176] (329)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
Mitochondrial Myopathies [MESH:D017240] (2176)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Muscular Disorders, Atrophic [MESH:D020966] (1598)
Muscular Dystrophies [MESH:D009136] (1593)	Muscular Dystrophy, Duchenne [MESH:D020388] (942)
	Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Myositis [MESH:D009220] (2071)	Polymyositis [MESH:D017285] (2007)
Myositis, Inclusion Body [MESH:D018979] (103)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Musculoskeletal Abnormalities [MESH:D009139] (3796)
Arthrogryposis [MESH:D001176] (329)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
Craniofacial Abnormalities [MESH:D019465] (3098)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Maxillofacial Abnormalities [MESH:D019767] (1447)
Jaw Abnormalities [MESH:D007569] (1438)	Cleft Palate [MESH:D002972] (1330)
Synostosis [MESH:D013580] (817)	Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)
Rheumatic Diseases [MESH:D012216] (4032)	Arthritis, Juvenile [MESH:D001171] (1060)
	Arthritis, Rheumatoid [MESH:D001172] (3603)
	Osteoarthritis [MESH:D010003] (1743)
C06. Digestive System Diseases	C06. Digestive System Diseases
Digestive System Diseases [MESH:D004066] (9461)
Biliary Tract Diseases [MESH:D001660] (3845)
Bile Duct Diseases [MESH:D001649] (3512)
Cholestasis [MESH:D002779] (3419)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
Cholelithiasis [MESH:D002769] (373)	Gallstones [MESH:D042882] (350)
Gallbladder Diseases [MESH:D005705] (1215)
Cholecystolithiasis [MESH:D041761] (353)	Gallstones [MESH:D042882] (350)
Digestive System Abnormalities [MESH:D004065] (2127)	Barrett Esophagus [MESH:D001471] (1930)
Digestive System Neoplasms [MESH:D004067] (7493)	Pancreatic Neoplasms [MESH:D010190] (3820)
Gastrointestinal Neoplasms [MESH:D005770] (6460)	Stomach Neoplasms [MESH:D013274] (4942)
Esophageal Neoplasms [MESH:D004938] (3737)	Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
	Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
Intestinal Neoplasms [MESH:D007414] (5359)
Colorectal Neoplasms [MESH:D015179] (5294)
Colonic Neoplasms [MESH:D003110] (4405)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Liver Neoplasms [MESH:D008113] (6048)	Carcinoma, Hepatocellular [MESH:D006528] (5375)
	Liver Neoplasms, Experimental [MESH:D008114] (2837)
Gastrointestinal Diseases [MESH:D005767] (7443)
Esophageal Diseases [MESH:D004935] (4255)	Barrett Esophagus [MESH:D001471] (1930)
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)
	Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
Gastroenteritis [MESH:D005759] (4066)
Colitis [MESH:D003092] (3199)	Colitis, Ulcerative [MESH:D003093] (2601)
Enterocolitis [MESH:D004760] (1536)	Enterocolitis, Necrotizing [MESH:D020345] (1367)
Inflammatory Bowel Diseases [MESH:D015212] (3492)	Colitis, Ulcerative [MESH:D003093] (2601)
	Crohn Disease [MESH:D003424] (2585)
Gastrointestinal Neoplasms [MESH:D005770] (6460)	Stomach Neoplasms [MESH:D013274] (4942)
Esophageal Neoplasms [MESH:D004938] (3737)	Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396)
	Adenocarcinoma Of Esophagus [MESH:C562730] (1530)
Intestinal Neoplasms [MESH:D007414] (5359)
Colorectal Neoplasms [MESH:D015179] (5294)
Colonic Neoplasms [MESH:D003110] (4405)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Intestinal Diseases [MESH:D007410] (6206)
Colonic Diseases [MESH:D003108] (5564)
Colitis [MESH:D003092] (3199)	Colitis, Ulcerative [MESH:D003093] (2601)
Colorectal Neoplasms [MESH:D015179] (5282)
Colonic Neoplasms [MESH:D003110] (4405)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Duodenal Diseases [MESH:D004378] (1982)
Peptic Ulcer [MESH:D010437] (1969)	Duodenal Ulcer [MESH:D004381] (1549)
Enterocolitis [MESH:D004760] (1536)	Enterocolitis, Necrotizing [MESH:D020345] (1367)
Inflammatory Bowel Diseases [MESH:D015212] (3492)	Colitis, Ulcerative [MESH:D003093] (2601)
	Crohn Disease [MESH:D003424] (2585)
Intestinal Neoplasms [MESH:D007414] (5359)
Colorectal Neoplasms [MESH:D015179] (5294)
Colonic Neoplasms [MESH:D003110] (4405)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Intestinal Polyposis [MESH:D044483] (1610)	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Rectal Diseases [MESH:D012002] (4596)	Colorectal Neoplasms [MESH:D015179] (4534)
Peptic Ulcer [MESH:D010437] (3172)	Duodenal Ulcer [MESH:D004381] (1549)
	Stomach Ulcer [MESH:D013276] (2915)
Stomach Diseases [MESH:D013272] (5325)	Stomach Neoplasms [MESH:D013274] (4942)
Peptic Ulcer [MESH:D010437] (2994)	Stomach Ulcer [MESH:D013276] (2915)
Liver Diseases [MESH:D008107] (8167)	Drug-Induced Liver Injury [MESH:D056486] (4936)
	Fatty Liver [MESH:D005234] (3584)
Hepatic Insufficiency [MESH:D048550] (2771)
Liver Failure [MESH:D017093] (2768)	Liver Failure, Acute [MESH:D017114] (2404)
Hepatitis [MESH:D006505] (3883)
Hepatitis, Chronic [MESH:D006521] (2071)	Hepatitis, Autoimmune [MESH:D019693] (1982)
Hepatitis, Viral, Human [MESH:D006525] (1766)	Hepatitis B [MESH:D006509] (976)
Liver Cirrhosis [MESH:D008103] (5542)	Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
	Liver Cirrhosis, Experimental [MESH:D008106] (4589)
Liver Diseases, Alcoholic [MESH:D008108] (3243)	Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
Liver Neoplasms [MESH:D008113] (6048)	Carcinoma, Hepatocellular [MESH:D006528] (5375)
	Liver Neoplasms, Experimental [MESH:D008114] (2837)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Pancreatic Diseases [MESH:D010182] (4453)	Pancreatic Neoplasms [MESH:D010190] (3820)
	Pancreatitis [MESH:D010195] (1924)
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)
Mouth Diseases [MESH:D009059] (4783)	Behcet Syndrome [MESH:D001528] (1784)
	Oral Submucous Fibrosis [MESH:D009914] (2432)
Lip Diseases [MESH:D008047] (924)	Cleft Lip [MESH:D002971] (914)
Mouth Abnormalities [MESH:D009056] (1383)	Cleft Lip [MESH:D002971] (914)
	Cleft Palate [MESH:D002972] (1330)
Mouth Neoplasms [MESH:D009062] (2263)	Leukoplakia, Oral [MESH:D007972] (921)
	Tongue Neoplasms [MESH:D014062] (1518)
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)
Mouth Abnormalities [MESH:D009056] (1383)	Cleft Lip [MESH:D002971] (914)
	Cleft Palate [MESH:D002972] (1330)
C08. Respiratory Tract Diseases	C08. Respiratory Tract Diseases
Respiratory Tract Diseases [MESH:D012140] (7881)
Bronchial Diseases [MESH:D001982] (4382)	Bronchial Hyperreactivity [MESH:D016535] (1357)
Asthma [MESH:D001249] (4098)	Asthma, Aspirin-Induced [MESH:D055963] (1055)
Lung Diseases [MESH:D008171] (7249)	Hypertension, Pulmonary [MESH:D006976] (2000)
	Pneumonia [MESH:D011014] (3482)
	Pulmonary Fibrosis [MESH:D011658] (3140)
	Tuberculosis, Pulmonary [MESH:D014397] (678)
Lung Diseases, Interstitial [MESH:D017563] (2966)
Pneumoconiosis [MESH:D011009] (2789)	Berylliosis [MESH:D001607] (2005)
Lung Diseases, Obstructive [MESH:D008173] (4697)	Asthma [MESH:D001249] (3903)
Lung Injury [MESH:D055370] (3688)
Pneumoconiosis [MESH:D011009] (2789)	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)
Pleural Diseases [MESH:D010995] (2240)	Pleurisy [MESH:D010998] (2070)
Respiratory Hypersensitivity [MESH:D012130] (4401)
Asthma [MESH:D001249] (4098)	Asthma, Aspirin-Induced [MESH:D055963] (1055)
Respiratory Tract Infections [MESH:D012141] (3926)	Influenza, Human [MESH:D007251] (1075)
	Pleurisy [MESH:D010998] (2070)
	Pneumonia [MESH:D011014] (3482)
	Tuberculosis, Pulmonary [MESH:D014397] (678)
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)
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)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Hearing Loss, Sensorineural [MESH:D006319] (1227)	Donnai-Barrow syndrome [MESH:C536390] (40)
Labyrinth Diseases [MESH:D007759] (846)	Vestibular Diseases [MESH:D015837] (819)
C10. Nervous System Diseases	C10. Nervous System Diseases
Z. Exceptions (4027)	Not Fully Specified [NFS] (4027)
Nervous System Diseases [MESH:D009422] (13325)
Central Nervous System Diseases [MESH:D002493] (9745)
Brain Diseases [MESH:D001927] (9294)	Brain Injuries [MESH:D001930] (3429)
Basal Ganglia Diseases [MESH:D001480] (4268)	Supranuclear Palsy, Progressive [MESH:D013494] (235)
Parkinsonian Disorders [MESH:D020734] (4009)	Lewy Body Disease [MESH:D020961] (1143)
	Parkinson Disease [MESH:D010300] (3595)
	Parkinson Disease, Secondary [MESH:D010302] (327)
Brain Diseases, Metabolic [MESH:D001928] (3351)
Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Galactosemias [MESH:D005693] (69)
	Leigh Disease [MESH:D007888] (206)
	Maple Syrup Urine Disease [MESH:D008375] (127)
Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)
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)
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)
Phenylketonurias [MESH:D010661] (156)	Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)
Cerebrovascular Disorders [MESH:D002561] (5542)	Carotid Artery Diseases [MESH:D002340] (1993)
	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Brain Ischemia [MESH:D002545] (4873)
Brain Infarction [MESH:D020520] (2571)
Cerebral Infarction [MESH:D002544] (2458)	Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
Intracranial Arterial Diseases [MESH:D020765] (2463)
Cerebral Arterial Diseases [MESH:D002539] (2440)	Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
Intracranial Hemorrhages [MESH:D020300] (3269)	Cerebral Hemorrhage [MESH:D002543] (2873)
Stroke [MESH:D020521] (3702)
Brain Infarction [MESH:D020520] (2571)
Cerebral Infarction [MESH:D002544] (2458)	Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
Dementia [MESH:D003704] (4498)	Alzheimer Disease [MESH:D000544] (4275)
	Lewy Body Disease [MESH:D020961] (1143)
Frontotemporal Lobar Degeneration [MESH:D057174] (310)
Frontotemporal Dementia [MESH:D057180] (300)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Epilepsy [MESH:D004827] (6274)	Seizures [MESH:D012640] (4502)
	Status Epilepticus [MESH:D013226] (4014)
Epilepsies, Partial [MESH:D004828] (1267)	Epilepsy, Temporal Lobe [MESH:D004833] (1108)
Epilepsy, Generalized [MESH:D004829] (1431)	Epilepsy, Tonic-Clonic [MESH:D004830] (1042)
Leukoencephalopathies [MESH:D056784] (1916)
Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)
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)
Central Nervous System Viral Diseases [MESH:D020805] (1416)
Meningitis, Viral [MESH:D008587] (1308)	Meningitis, Aseptic [MESH:D008582] (1305)
Meningitis [MESH:D008581] (1506)	Meningitis, Aseptic [MESH:D008582] (1305)
Meningitis, Viral [MESH:D008587] (1308)	Meningitis, Aseptic [MESH:D008582] (1305)
Movement Disorders [MESH:D009069] (4823)	Supranuclear Palsy, Progressive [MESH:D013494] (235)
Dyskinesias [MESH:D020820] (1827)	Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)
	Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Dystonic Disorders [MESH:D020821] (729)	Dystonia, Dopa-responsive [MESH:C538007] (98)
Parkinsonian Disorders [MESH:D020734] (4009)	Lewy Body Disease [MESH:D020961] (1143)
	Parkinson Disease [MESH:D010300] (3595)
	Parkinson Disease, Secondary [MESH:D010302] (327)
Spinal Cord Diseases [MESH:D013118] (4376)	Spinal Cord Compression [MESH:D013117] (1800)
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)	Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
Cranial Nerve Diseases [MESH:D003389] (2004)
Ocular Motility Disorders [MESH:D015835] (1697)
Ophthalmoplegia [MESH:D009886] (1468)	Supranuclear Palsy, Progressive [MESH:D013494] (235)
Demyelinating Diseases [MESH:D003711] (2917)
Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)
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)	Donnai-Barrow syndrome [MESH:C536390] (40)
Central Nervous System Vascular Malformations [MESH:D020785] (1031)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Neural Tube Defects [MESH:D009436] (2143)	Spinal Dysraphism [MESH:D016135] (1025)
Neurodegenerative Diseases [MESH:D019636] (6613)	Lewy Body Disease [MESH:D020961] (1143)
	Parkinson Disease [MESH:D010300] (3595)
Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)
Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)	Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)
Motor Neuron Disease [MESH:D016472] (3670)
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)	Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
Tauopathies [MESH:D024801] (4289)	Alzheimer Disease [MESH:D000544] (4275)
	Supranuclear Palsy, Progressive [MESH:D013494] (235)
TDP-43 Proteinopathies [MESH:D057177] (3337)
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)	Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
Frontotemporal Lobar Degeneration [MESH:D057174] (308)
Frontotemporal Dementia [MESH:D057180] (298)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Neurologic Manifestations [MESH:D009461] (8964)	Neurogenic Inflammation [MESH:D020078] (2246)
	Seizures [MESH:D012640] (4514)
Dyskinesias [MESH:D020820] (3365)	Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)
	Dystonia [MESH:D004421] (848)
	Hypokinesia [MESH:D018476] (279)
Neurobehavioral Manifestations [MESH:D019954] (5230)
Communication Disorders [MESH:D003147] (2918)	Learning Disorders [MESH:D007859] (2727)
Memory Disorders [MESH:D008569] (3233)	Amnesia [MESH:D000647] (1911)
Intellectual Disability [MESH:D008607] (3054)
Mental Retardation, X-Linked [MESH:D038901] (1854)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Mental Retardation, X-Linked 17 [MESH:C563140] (41)
	Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)
Neuromuscular Manifestations [MESH:D020879] (2130)
Muscle Hypertonia [MESH:D009122] (775)	Muscle Rigidity [MESH:D009127] (617)
Pain [MESH:D010146] (3875)	Headache [MESH:D006261] (1416)
Paralysis [MESH:D010243] (2043)
Ophthalmoplegia [MESH:D009886] (1468)	Supranuclear Palsy, Progressive [MESH:D013494] (235)
Sensation Disorders [MESH:D012678] (5011)
Hearing Disorders [MESH:D006311] (2103)
Hearing Loss [MESH:D034381] (2068)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Hearing Loss, Sensorineural [MESH:D006319] (1227)	Donnai-Barrow syndrome [MESH:C536390] (40)
Somatosensory Disorders [MESH:D020886] (4000)	Hyperalgesia [MESH:D006930] (3929)
Neuromuscular Diseases [MESH:D009468] (7336)
Motor Neuron Disease [MESH:D016472] (3670)
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)	Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
Muscular Diseases [MESH:D009135] (3538)	VLCAD deficiency [MESH:C536353] (55)
Muscular Disorders, Atrophic [MESH:D020966] (1594)
Muscular Dystrophies [MESH:D009136] (1589)	Muscular Dystrophy, Duchenne [MESH:D020388] (942)
	Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Mitochondrial Myopathies [MESH:D017240] (2176)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Myositis [MESH:D009220] (2069)	Polymyositis [MESH:D017285] (2007)
Myositis, Inclusion Body [MESH:D018979] (103)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Peripheral Nervous System Diseases [MESH:D010523] (6151)	Polyneuropathies [MESH:D011115] (1134)
Neurotoxicity Syndromes [MESH:D020258] (4570)	Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Heavy Metal Poisoning, Nervous System [MESH:D020260] (2912)	Arsenic Poisoning [MESH:D020261] (2540)
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)	Eye Diseases, Hereditary [MESH:D015785] (1869)
Lens Diseases [MESH:D007905] (900)
Cataract [MESH:D002386] (860)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Ocular Hypertension [MESH:D009798] (1630)
Glaucoma [MESH:D005901] (1458)	Glaucoma, Open-Angle [MESH:D005902] (1281)
Ocular Motility Disorders [MESH:D015835] (1699)
Ophthalmoplegia [MESH:D009886] (1468)	Supranuclear Palsy, Progressive [MESH:D013494] (235)
Refractive Errors [MESH:D012030] (457)
Myopia [MESH:D009216] (349)	Donnai-Barrow syndrome [MESH:C536390] (40)
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)	Prostatic Neoplasms [MESH:D011471] (6135)
Infertility [MESH:D007246] (2909)	Infertility, Male [MESH:D007248] (2851)
Penile Diseases [MESH:D010409] (1805)	Hypospadias [MESH:D007021] (798)
Prostatic Diseases [MESH:D011469] (6204)	Prostatic Neoplasms [MESH:D011471] (6135)
Urogenital Abnormalities [MESH:D014564] (2065)	Hypospadias [MESH:D007021] (798)
Disorders of Sex Development [MESH:D012734] (1637)
Adrenogenital Syndrome [MESH:D047808] (715)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
Urogenital Neoplasms [MESH:D014565] (6932)
Genital Neoplasms, Male [MESH:D005834] (6224)	Prostatic Neoplasms [MESH:D011471] (6135)
Urologic Neoplasms [MESH:D014571] (5315)	Urinary Bladder Neoplasms [MESH:D001749] (4079)
Kidney Neoplasms [MESH:D007680] (3966)	Carcinoma, Renal Cell [MESH:D002292] (2975)
Urologic Diseases [MESH:D014570] (7792)
Kidney Diseases [MESH:D007674] (7242)	Diabetic Nephropathies [MESH:D003928] (2301)
	Hydronephrosis [MESH:D006869] (956)
	Hyperoxaluria [MESH:D006959] (1498)
Kidney Neoplasms [MESH:D007680] (3966)	Carcinoma, Renal Cell [MESH:D002292] (2975)
Nephritis [MESH:D009393] (4236)	Nephritis, Interstitial [MESH:D009395] (1927)
Glomerulonephritis [MESH:D005921] (3758)	Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
Nephrosis [MESH:D009401] (2228)	Nephrotic Syndrome [MESH:D009404] (1536)
Renal Insufficiency [MESH:D051437] (4951)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
	Acute Kidney Injury [MESH:D058186] (4142)
Renal Insufficiency, Chronic [MESH:D051436] (2931)	Kidney Failure, Chronic [MESH:D007676] (2930)
Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)	Donnai-Barrow syndrome [MESH:C536390] (40)
Uremia [MESH:D014511] (2898)	Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
Urethral Diseases [MESH:D014522] (955)
Urethral Obstruction [MESH:D014524] (937)	Urinary Bladder Neck Obstruction [MESH:D001748] (924)
Urinary Bladder Diseases [MESH:D001745] (4374)	Urinary Bladder Neck Obstruction [MESH:D001748] (924)
	Urinary Bladder Neoplasms [MESH:D001749] (4079)
Urination Disorders [MESH:D014555] (3598)
Proteinuria [MESH:D011507] (3293)	Donnai-Barrow syndrome [MESH:C536390] (40)
	Albuminuria [MESH:D000419] (2394)
C13. Female Urogenital Diseases and Pregnancy Complications	C13. Female Urogenital Diseases and Pregnancy Complications
Z. Exceptions (1116)	Not Fully Specified [NFS] (1116)
Female Urogenital Diseases [MESH:D052776] (8724)
Genital Diseases, Female [MESH:D005831] (5563)	Endometriosis [MESH:D004715] (2461)
Adnexal Diseases [MESH:D000291] (4273)
Ovarian Diseases [MESH:D010049] (4255)	Ovarian Neoplasms [MESH:D010051] (3281)
Infertility [MESH:D007246] (2211)	Infertility, Female [MESH:D007247] (2184)
Uterine Diseases [MESH:D014591] (2479)	Endometrial Hyperplasia [MESH:D004714] (263)
Uterine Neoplasms [MESH:D014594] (2430)	Endometrial Neoplasms [MESH:D016889] (1984)
Urogenital Abnormalities [MESH:D014564] (2043)	Hypospadias [MESH:D007021] (798)
Disorders of Sex Development [MESH:D012734] (1637)
Adrenogenital Syndrome [MESH:D047808] (715)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
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)	Carcinoma, Renal Cell [MESH:D002292] (2975)
Urologic Diseases [MESH:D014570] (7793)
Kidney Diseases [MESH:D007674] (7242)	Diabetic Nephropathies [MESH:D003928] (2301)
	Hydronephrosis [MESH:D006869] (956)
	Hyperoxaluria [MESH:D006959] (1498)
Kidney Neoplasms [MESH:D007680] (3966)	Carcinoma, Renal Cell [MESH:D002292] (2975)
Nephritis [MESH:D009393] (4236)	Nephritis, Interstitial [MESH:D009395] (1927)
Glomerulonephritis [MESH:D005921] (3758)	Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754)
Nephrosis [MESH:D009401] (2228)	Nephrotic Syndrome [MESH:D009404] (1536)
Renal Insufficiency [MESH:D051437] (4951)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
	Acute Kidney Injury [MESH:D058186] (4142)
Renal Insufficiency, Chronic [MESH:D051436] (2931)	Kidney Failure, Chronic [MESH:D007676] (2930)
Renal Tubular Transport, Inborn Errors [MESH:D015499] (1058)	Donnai-Barrow syndrome [MESH:C536390] (40)
Uremia [MESH:D014511] (2898)	Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
Urethral Diseases [MESH:D014522] (955)
Urethral Obstruction [MESH:D014524] (937)	Urinary Bladder Neck Obstruction [MESH:D001748] (924)
Urinary Bladder Diseases [MESH:D001745] (4375)	Urinary Bladder Neck Obstruction [MESH:D001748] (924)
	Urinary Bladder Neoplasms [MESH:D001749] (4079)
Urination Disorders [MESH:D014555] (3598)
Proteinuria [MESH:D011507] (3293)	Donnai-Barrow syndrome [MESH:C536390] (40)
	Albuminuria [MESH:D000419] (2394)
Pregnancy Complications [MESH:D011248] (4768)	Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
Abortion, Spontaneous [MESH:D000022] (2780)	Embryo Loss [MESH:D020964] (288)
Hypertension, Pregnancy-Induced [MESH:D046110] (1453)	Pre-Eclampsia [MESH:D011225] (1435)
Obstetric Labor Complications [MESH:D007744] (1550)	Obstetric Labor, Premature [MESH:D007752] (1316)
C14. Cardiovascular Diseases	C14. Cardiovascular Diseases
Z. Exceptions (2667)	Not Fully Specified [NFS] (2667)
Cardiovascular Diseases [MESH:D002318] (10123)	Pregnancy Complications, Cardiovascular [MESH:D011249] (1994)
Cardiovascular Abnormalities [MESH:D018376] (3153)
Heart Defects, Congenital [MESH:D006330] (2447)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Ductus Arteriosus, Patent [MESH:D004374] (325)	Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
Vascular Malformations [MESH:D054079] (1098)
Arteriovenous Malformations [MESH:D001165] (1058)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Central Nervous System Vascular Malformations [MESH:D020785] (1031)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Heart Diseases [MESH:D006331] (8614)	Arrhythmias, Cardiac [MESH:D001145] (4679)
	Heart Failure [MESH:D006333] (4058)
	Pericardial Effusion [MESH:D010490] (1015)
Cardiomegaly [MESH:D006332] (4081)	Hypertrophy, Left Ventricular [MESH:D017379] (1430)
Cardiomyopathy, Dilated [MESH:D002311] (1576)	Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)
Cardiomyopathies [MESH:D009202] (5331)	Cardiomyopathy, Hypertrophic [MESH:D002312] (1516)
	Myocardial Reperfusion Injury [MESH:D015428] (3500)
Cardiomyopathy, Dilated [MESH:D002311] (1576)	Cardiomyopathy, Dilated, 1t [MESH:C566052] (76)
Heart Defects, Congenital [MESH:D006330] (2443)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Ductus Arteriosus, Patent [MESH:D004374] (325)	Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
Heart Valve Diseases [MESH:D006349] (3333)	Aortic Valve Insufficiency [MESH:D001022] (1002)
Aortic Valve Stenosis [MESH:D001024] (1742)
Aortic Stenosis, Subvalvular [MESH:D001020] (1455)	Cardiomyopathy, Hypertrophic [MESH:D002312] (1451)
Myocardial Ischemia [MESH:D017202] (5787)	Acute Coronary Syndrome [MESH:D054058] (2286)
	Myocardial 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)
Ventricular Dysfunction [MESH:D018754] (2348)	Ventricular Dysfunction, Left [MESH:D018487] (1631)
Vascular Diseases [MESH:D014652] (8691)	Hyperemia [MESH:D006940] (2372)
	Hypotension [MESH:D007022] (4045)
	Varicose Veins [MESH:D014648] (383)
Aneurysm [MESH:D000783] (1886)
Aortic Aneurysm [MESH:D001014] (1721)	Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
Aortic Aneurysm, Thoracic [MESH:D017545] (781)	Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
Aortic Diseases [MESH:D001018] (1737)
Aortic Aneurysm [MESH:D001014] (1721)	Aortic Aneurysm, Abdominal [MESH:D017544] (1519)
Aortic Aneurysm, Thoracic [MESH:D017545] (781)	Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
Arterial Occlusive Diseases [MESH:D001157] (4520)
Arteriosclerosis [MESH:D001161] (4466)	Atherosclerosis [MESH:D050197] (4188)
	Coronary Artery Disease [MESH:D003324] (2685)
Arteriovenous Malformations [MESH:D001165] (1058)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Cerebrovascular Disorders [MESH:D002561] (5541)	Carotid Artery Diseases [MESH:D002340] (1993)
Brain Ischemia [MESH:D002545] (4873)
Brain Infarction [MESH:D020520] (2571)
Cerebral Infarction [MESH:D002544] (2458)	Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
Intracranial Arterial Diseases [MESH:D020765] (2468)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Cerebral Arterial Diseases [MESH:D002539] (2440)	Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
Intracranial Hemorrhages [MESH:D020300] (3269)	Cerebral Hemorrhage [MESH:D002543] (2873)
Stroke [MESH:D020521] (3702)
Brain Infarction [MESH:D020520] (2571)
Cerebral Infarction [MESH:D002544] (2458)	Infarction, Middle Cerebral Artery [MESH:D020244] (2268)
Embolism and Thrombosis [MESH:D016769] (3374)	Thrombosis [MESH:D013927] (3101)
Hemostatic Disorders [MESH:D020141] (2894)	Multiple Myeloma [MESH:D009101] (2765)
Hypertension [MESH:D006973] (5655)	Hypertension, Essential [MESH:C562386] (1308)
Myocardial Ischemia [MESH:D017202] (5791)	Acute Coronary Syndrome [MESH:D054058] (2286)
	Myocardial 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)
C15. Hemic and Lymphatic Diseases	C15. Hemic and Lymphatic Diseases
Hematologic Diseases [MESH:D006402] (6174)
Anemia [MESH:D000740] (3966)
Anemia, Aplastic [MESH:D000741] (1925)
Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)
Anemia, Diamond-Blackfan [MESH:D029503] (158)	Diamond-Blackfan Anemia 9 [MESH:C567650] (43)
Anemia, Hemolytic [MESH:D000743] (3083)	Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
Anemia, Hemolytic, Congenital [MESH:D000745] (2001)	Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)
Red-Cell Aplasia, Pure [MESH:D012010] (183)
Anemia, Diamond-Blackfan [MESH:D029503] (158)	Diamond-Blackfan Anemia 9 [MESH:C567650] (43)
Blood Platelet Disorders [MESH:D001791] (3174)
Thrombocytopenia [MESH:D013921] (2966)
Thrombotic Microangiopathies [MESH:D057049] (2598)	Hemolytic-Uremic Syndrome [MESH:D006463] (2435)
Blood Protein Disorders [MESH:D001796] (3051)
Hypoproteinemia [MESH:D007019] (1335)	Hypoalbuminemia [MESH:D034141] (1332)
Paraproteinemias [MESH:D010265] (2781)	Multiple Myeloma [MESH:D009101] (2765)
Bone Marrow Diseases [MESH:D001855] (2944)	Myelodysplastic Syndromes [MESH:D009190] (2093)
Anemia, Aplastic [MESH:D000741] (1925)
Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)
Anemia, Diamond-Blackfan [MESH:D029503] (158)	Diamond-Blackfan Anemia 9 [MESH:C567650] (43)
Hemorrhagic Disorders [MESH:D006474] (3359)	Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328)
Hemostatic Disorders [MESH:D020141] (2932)	Multiple Myeloma [MESH:D009101] (2765)
Leukocyte Disorders [MESH:D007960] (2662)
Leukopenia [MESH:D007970] (1921)
Agranulocytosis [MESH:D000380] (1675)	Neutropenia [MESH:D009503] (1629)
Lymphatic Diseases [MESH:D008206] (5167)
Lymphatic Abnormalities [MESH:D044148] (251)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Lymphoproliferative Disorders [MESH:D008232] (4638)	Giant Lymph Node Hyperplasia [MESH:D005871] (1013)
Leukemia, Lymphoid [MESH:D007945] (3047)	Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)
Leukemia, B-Cell [MESH:D015448] (2564)	Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
Lymphoma [MESH:D008223] (3684)
Lymphoma, Non-Hodgkin [MESH:D008228] (3330)	Burkitt Lymphoma [MESH:D002051] (691)
Lymphoma, B-Cell [MESH:D016393] (2624)	Burkitt Lymphoma [MESH:D002051] (691)
	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)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Cardiovascular Abnormalities [MESH:D018376] (3294)
Heart Defects, Congenital [MESH:D006330] (2611)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Ductus Arteriosus, Patent [MESH:D004374] (325)	Aortic aneurysm, familial thoracic 4 [MESH:C537784] (29)
Vascular Malformations [MESH:D054079] (1108)
Arteriovenous Malformations [MESH:D001165] (1058)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Central Nervous System Vascular Malformations [MESH:D020785] (1018)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Chromosome Disorders [MESH:D025063] (2030)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Lymphatic Abnormalities [MESH:D044148] (251)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Musculoskeletal Abnormalities [MESH:D009139] (3779)
Arthrogryposis [MESH:D001176] (329)	Arthrogryposis renal dysfunction cholestasis syndrome [MESH:C535382] (23)
Craniofacial Abnormalities [MESH:D019465] (3064)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Maxillofacial Abnormalities [MESH:D019767] (1448)
Jaw Abnormalities [MESH:D007569] (1435)	Cleft Palate [MESH:D002972] (1330)
Synostosis [MESH:D013580] (817)	Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)
Nervous System Malformations [MESH:D009421] (3354)
Agenesis of Corpus Callosum [MESH:D061085] (345)	Donnai-Barrow syndrome [MESH:C536390] (40)
Central Nervous System Vascular Malformations [MESH:D020785] (1031)	Intracranial Arteriovenous Malformations [MESH:D002538] (1015)
Neural Tube Defects [MESH:D009436] (2143)	Spinal Dysraphism [MESH:D016135] (1025)
Skin Abnormalities [MESH:D012868] (1723)
Ichthyosis [MESH:D007057] (481)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Stomatognathic System Abnormalities [MESH:D018640] (1705)
Maxillofacial Abnormalities [MESH:D019767] (1447)
Jaw Abnormalities [MESH:D007569] (1438)	Cleft Palate [MESH:D002972] (1330)
Mouth Abnormalities [MESH:D009056] (1383)	Cleft Lip [MESH:D002971] (914)
	Cleft Palate [MESH:D002972] (1330)
Urogenital Abnormalities [MESH:D014564] (2064)	Hypospadias [MESH:D007021] (798)
Disorders of Sex Development [MESH:D012734] (1637)
Adrenogenital Syndrome [MESH:D047808] (715)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
Genetic Diseases, Inborn [MESH:D030342] (9766)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
	Eye Diseases, Hereditary [MESH:D015785] (1867)
	Pycnodysostosis [MESH:D058631] (73)
Anemia, Hemolytic, Congenital [MESH:D000745] (2001)	Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)
Anemia, Hypoplastic, Congenital [MESH:D029502] (1665)
Anemia, Diamond-Blackfan [MESH:D029503] (158)	Diamond-Blackfan Anemia 9 [MESH:C567650] (43)
Chromosome Disorders [MESH:D025063] (2030)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Genetic Diseases, X-Linked [MESH:D040181] (3028)	Chondrodysplasia punctata 2, X-linked dominant [MESH:C538416] (61)
	Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)
	Muscular Dystrophy, Duchenne [MESH:D020388] (942)
Mental Retardation, X-Linked [MESH:D038901] (1867)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Mental Retardation, X-Linked 17 [MESH:C563140] (41)
	Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)
Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)
Mental Retardation, X-Linked [MESH:D038901] (1848)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Mental Retardation, X-Linked 17 [MESH:C563140] (41)
	Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)
Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)	Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)
Metabolism, Inborn Errors [MESH:D008661] (6032)	Mitochondrial Complex II Deficiency [MESH:C565375] (66)
	Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)
Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565)	Beta ketothiolase deficiency [MESH:C535434] (65)
	Maple Syrup Urine Disease [MESH:D008375] (127)
Hyperhomocysteinemia [MESH:D020138] (1724)	Gamma-cystathionase deficiency [MESH:C535408] (106)
Phenylketonurias [MESH:D010661] (156)	Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)
Amyloidosis, Familial [MESH:D028226] (696)	Amyloidosis, familial visceral [MESH:C538249] (285)
Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Galactosemias [MESH:D005693] (69)
	Leigh Disease [MESH:D007888] (206)
	Maple Syrup Urine Disease [MESH:D008375] (127)
Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)
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)
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)
Phenylketonurias [MESH:D010661] (156)	Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)
Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)	Galactosemias [MESH:D005693] (69)
Glycogen Storage Disease [MESH:D006008] (530)	Glycogen Storage Disease IC [MESH:C562805] (53)
Glycogen Storage Disease Type I [MESH:D005953] (140)	Glycogen Storage Disease IB [MESH:C562594] (53)
Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)	Leigh Disease [MESH:D007888] (206)
Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)	Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency [MESH:C536080] (41)
	VLCAD deficiency [MESH:C536353] (55)
Lipidoses [MESH:D008064] (1655)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)	Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)
Sphingolipidoses [MESH:D013106] (582)
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)	Pycnodysostosis [MESH:D058631] (73)
Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)
Sphingolipidoses [MESH:D013106] (582)
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)
Porphyrias [MESH:D011164] (917)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Renal Tubular Transport, Inborn Errors [MESH:D015499] (1027)	Donnai-Barrow syndrome [MESH:C536390] (40)
Steroid Metabolism, Inborn Errors [MESH:D043202] (962)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
	Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)
Muscular Dystrophies [MESH:D009136] (1597)	Muscular Dystrophy, Duchenne [MESH:D020388] (942)
	Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854)
Muscular Dystrophies, Limb-Girdle [MESH:D049288] (259)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Neoplastic Syndromes, Hereditary [MESH:D009386] (2578)	Hemangioma, capillary infantile [MESH:C535860] (190)
	Adenomatous Polyposis Coli [MESH:D011125] (1565)
Skin Diseases, Genetic [MESH:D012873] (3456)	Dermatitis, Atopic [MESH:D003876] (2052)
	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Infant, Newborn, Diseases [MESH:D007232] (3064)	Asphyxia Neonatorum [MESH:D001238] (1648)
Ichthyosis [MESH:D007057] (476)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
C17. Skin and Connective Tissue Diseases	C17. Skin and Connective Tissue Diseases
Connective Tissue Diseases [MESH:D003240] (4490)	Lupus Erythematosus, Systemic [MESH:D008180] (2317)
	Scleroderma, Systemic [MESH:D012595] (199)
Collagen Diseases [MESH:D003095] (1267)	Keloid [MESH:D007627] (1111)
Rheumatic Diseases [MESH:D012216] (3619)	Arthritis, Juvenile [MESH:D001171] (1060)
	Arthritis, Rheumatoid [MESH:D001172] (3603)
Skin Diseases [MESH:D012871] (8774)	Scleroderma, Systemic [MESH:D012595] (199)
	Skin Neoplasms [MESH:D012878] (2991)
Acneiform Eruptions [MESH:D017486] (1312)	Chloracne [MESH:D054506] (1274)
Breast Diseases [MESH:D001941] (6148)
Breast Neoplasms [MESH:D001943] (6077)	Carcinoma, Ductal, Breast [MESH:D018270] (1112)
Dermatitis [MESH:D003872] (4530)	Dermatitis, Atopic [MESH:D003876] (2052)
Dermatitis, Contact [MESH:D003877] (3394)	Dermatitis, Allergic Contact [MESH:D017449] (3241)
Facial Dermatoses [MESH:D005148] (1336)
Acneiform Eruptions [MESH:D017486] (1312)	Chloracne [MESH:D054506] (1274)
Hair Diseases [MESH:D006201] (1891)
Hypotrichosis [MESH:D007039] (1513)	Alopecia [MESH:D000505] (1453)
Keratosis [MESH:D007642] (1941)
Ichthyosis [MESH:D007057] (481)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Skin Abnormalities [MESH:D012868] (1709)
Ichthyosis [MESH:D007057] (481)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Skin Diseases, Eczematous [MESH:D017443] (3740)	Dermatitis, Atopic [MESH:D003876] (2052)
Dermatitis, Contact [MESH:D003877] (3394)	Dermatitis, Allergic Contact [MESH:D017449] (3241)
Skin Diseases, Genetic [MESH:D012873] (3481)	Dermatitis, Atopic [MESH:D003876] (2052)
	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Skin Diseases, Infectious [MESH:D012874] (2684)
Skin Diseases, Parasitic [MESH:D012876] (2526)
Leishmaniasis [MESH:D007896] (2516)	Leishmaniasis, Cutaneous [MESH:D016773] (2359)
Skin Diseases, Metabolic [MESH:D012875] (1574)
Porphyrias [MESH:D011164] (917)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Skin Diseases, Papulosquamous [MESH:D017444] (3392)	Lichenoid Eruptions [MESH:D017512] (1324)
	Psoriasis [MESH:D011565] (3278)
Skin Diseases, Vascular [MESH:D017445] (3288)	Behcet Syndrome [MESH:D001528] (1784)
C18. Nutritional and Metabolic Diseases	C18. Nutritional and Metabolic Diseases
Metabolic Diseases [MESH:D008659] (9025)	Metabolic Syndrome X [MESH:D024821] (2151)
Brain Diseases, Metabolic [MESH:D001928] (3350)
Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Galactosemias [MESH:D005693] (69)
	Leigh Disease [MESH:D007888] (206)
	Maple Syrup Urine Disease [MESH:D008375] (127)
Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)
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)
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)
Phenylketonurias [MESH:D010661] (156)	Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)
Calcium Metabolism Disorders [MESH:D002128] (3634)	Calcinosis [MESH:D002114] (2989)
	Hypercalcemia [MESH:D006934] (1999)
Glucose Metabolism Disorders [MESH:D044882] (6122)	Hyperglycemia [MESH:D006943] (1858)
Diabetes Mellitus [MESH:D003920] (5891)	Diabetes Mellitus, Experimental [MESH:D003921] (4771)
	Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
Diabetes Mellitus, Type 1 [MESH:D003922] (1897)	Wolcott-Rallison syndrome [MESH:C536739] (92)
Hyperinsulinism [MESH:D006946] (3586)
Insulin Resistance [MESH:D007333] (3511)	Metabolic Syndrome X [MESH:D024821] (2151)
Lipid Metabolism Disorders [MESH:D052439] (3225)
Dyslipidemias [MESH:D050171] (2428)
Hyperlipidemias [MESH:D006949] (1908)	Hypercholesterolemia [MESH:D006937] (1404)
Lipid Metabolism, Inborn Errors [MESH:D008052] (461)	Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency [MESH:C536080] (41)
	VLCAD deficiency [MESH:C536353] (55)
Lipidoses [MESH:D008064] (1655)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)	Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)
Sphingolipidoses [MESH:D013106] (582)
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)
Malabsorption Syndromes [MESH:D008286] (1869)
Hyperhomocysteinemia [MESH:D020138] (1716)	Gamma-cystathionase deficiency [MESH:C535408] (106)
Metabolism, Inborn Errors [MESH:D008661] (6028)	Mitochondrial Complex II Deficiency [MESH:C565375] (66)
	Phosphoglycerate Kinase 1 Deficiency [MESH:C567067] (98)
Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559)	Beta ketothiolase deficiency [MESH:C535434] (65)
	Maple Syrup Urine Disease [MESH:D008375] (127)
Hyperhomocysteinemia [MESH:D020138] (1724)	Gamma-cystathionase deficiency [MESH:C535408] (106)
Phenylketonurias [MESH:D010661] (156)	Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)
Amyloidosis, Familial [MESH:D028226] (696)	Amyloidosis, familial visceral [MESH:C538249] (285)
Brain Diseases, Metabolic, Inborn [MESH:D020739] (2634)	Creatine deficiency, X-linked [MESH:C535598] (58)
	Galactosemias [MESH:D005693] (69)
	Leigh Disease [MESH:D007888] (206)
	Maple Syrup Urine Disease [MESH:D008375] (127)
Hereditary Central Nervous System Demyelinating Diseases [MESH:D020279] (1497)
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)
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)
Phenylketonurias [MESH:D010661] (156)	Hyperphenylalaninemia, BH4-Deficient, B [MESH:C562656] (97)
Carbohydrate Metabolism, Inborn Errors [MESH:D002239] (1100)	Galactosemias [MESH:D005693] (69)
Glycogen Storage Disease [MESH:D006008] (530)	Glycogen Storage Disease IC [MESH:C562805] (53)
Glycogen Storage Disease Type I [MESH:D005953] (140)	Glycogen Storage Disease IB [MESH:C562594] (53)
Pyruvate Metabolism, Inborn Errors [MESH:D015323] (324)	Leigh Disease [MESH:D007888] (206)
Lipid Metabolism, Inborn Errors [MESH:D008052] (2071)	Hydroxyacyl-CoA Dehydrogenase, Type 2, Deficiency [MESH:C536080] (41)
	VLCAD deficiency [MESH:C536353] (55)
Lipidoses [MESH:D008064] (1655)	Sjogren-Larsson Syndrome [MESH:D016111] (67)
Neuronal Ceroid-Lipofuscinoses [MESH:D009472] (1026)	Ceroid Lipofuscinosis, Neuronal, 10 [MESH:C566438] (159)
Sphingolipidoses [MESH:D013106] (582)
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)	Pycnodysostosis [MESH:D058631] (73)
Lysosomal Storage Diseases, Nervous System [MESH:D020140] (636)
Sphingolipidoses [MESH:D013106] (582)
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)
Porphyrias [MESH:D011164] (917)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Renal Tubular Transport, Inborn Errors [MESH:D015499] (1026)	Donnai-Barrow syndrome [MESH:C536390] (40)
Steroid Metabolism, Inborn Errors [MESH:D043202] (962)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
	Antley-Bixler Syndrome Phenotype [MESH:D054882] (284)
Mitochondrial Diseases [MESH:D028361] (2561)	VLCAD deficiency [MESH:C536353] (55)
	Mitochondrial Complex II Deficiency [MESH:C565375] (66)
	Leigh Disease [MESH:D007888] (206)
Mitochondrial Myopathies [MESH:D017240] (2176)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Porphyrias [MESH:D011164] (917)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Proteostasis Deficiencies [MESH:D057165] (3522)
Amyloidosis [MESH:D000686] (791)
Amyloidosis, Familial [MESH:D028226] (696)	Amyloidosis, familial visceral [MESH:C538249] (285)
TDP-43 Proteinopathies [MESH:D057177] (3337)
Amyotrophic Lateral Sclerosis [MESH:D000690] (3296)	Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559)
Frontotemporal Lobar Degeneration [MESH:D057174] (308)
Frontotemporal Dementia [MESH:D057180] (298)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Skin Diseases, Metabolic [MESH:D012875] (1574)
Porphyrias [MESH:D011164] (917)
Porphyrias, Hepatic [MESH:D017094] (881)	Porphyria, Acute Intermittent [MESH:D017118] (61)
Wasting Syndrome [MESH:D019282] (1959)	HIV Wasting Syndrome [MESH:D019247] (1956)
Water-Electrolyte Imbalance [MESH:D014883] (2790)	Hypercalcemia [MESH:D006934] (1999)
Nutrition Disorders [MESH:D009748] (4945)
Malnutrition [MESH:D044342] (2754)
Deficiency Diseases [MESH:D003677] (2742)
Avitaminosis [MESH:D001361] (2304)	Vitamin D Deficiency [MESH:D014808] (360)
Vitamin B Deficiency [MESH:D014804] (1817)
Hyperhomocysteinemia [MESH:D020138] (1716)	Gamma-cystathionase deficiency [MESH:C535408] (106)
Overnutrition [MESH:D044343] (4463)	Obesity [MESH:D009765] (4462)
Wasting Syndrome [MESH:D019282] (1959)	HIV Wasting Syndrome [MESH:D019247] (1956)
C19. Endocrine System Diseases	C19. Endocrine System Diseases
Endocrine System Diseases [MESH:D004700] (8062)
Adrenal Gland Diseases [MESH:D000307] (2397)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
Adrenocortical Hyperfunction [MESH:D000308] (618)	Hyperaldosteronism [MESH:D006929] (419)
Diabetes Mellitus [MESH:D003920] (6159)	Diabetes Mellitus, Experimental [MESH:D003921] (4771)
	Diabetes Mellitus, Type 2 [MESH:D003924] (4219)
Diabetes Complications [MESH:D048909] (4129)	Diabetic Nephropathies [MESH:D003928] (2301)
Diabetes Mellitus, Type 1 [MESH:D003922] (1897)	Wolcott-Rallison syndrome [MESH:C536739] (92)
Endocrine Gland Neoplasms [MESH:D004701] (4925)	Ovarian Neoplasms [MESH:D010051] (3275)
	Pancreatic Neoplasms [MESH:D010190] (3820)
	Thyroid Neoplasms [MESH:D013964] (2040)
Gonadal Disorders [MESH:D006058] (5088)	Puberty, Precocious [MESH:D011629] (1147)
Disorders of Sex Development [MESH:D012734] (1637)
Adrenogenital Syndrome [MESH:D047808] (715)	Adrenal Hyperplasia, Congenital [MESH:D000312] (674)
Ovarian Diseases [MESH:D010049] (4253)	Ovarian Neoplasms [MESH:D010051] (3281)
Parathyroid Diseases [MESH:D010279] (1604)
Hyperparathyroidism [MESH:D006961] (1475)	Hyperparathyroidism, Secondary [MESH:D006962] (1138)
Hypoparathyroidism [MESH:D007011] (376)
22q11 Deletion Syndrome [MESH:D058165] (237)	DiGeorge Syndrome [MESH:D004062] (236)
Thyroid Diseases [MESH:D013959] (2808)	Thyroid Neoplasms [MESH:D013964] (2040)
C20. Immune System Diseases	C20. Immune System Diseases
Immune System Diseases [MESH:D007154] (7674)
Autoimmune Diseases [MESH:D001327] (5067)	Spondyloenchondrodysplasia [MESH:C535782] (71)
	Arthritis, Juvenile [MESH:D001171] (1060)
	Arthritis, Rheumatoid [MESH:D001172] (3601)
	Hepatitis, Autoimmune [MESH:D019693] (1982)
	Lupus Erythematosus, Systemic [MESH:D008180] (2317)
Diabetes Mellitus, Type 1 [MESH:D003922] (1893)	Wolcott-Rallison syndrome [MESH:C536739] (92)
Hypersensitivity [MESH:D006967] (5873)
Drug Hypersensitivity [MESH:D004342] (4000)	Asthma, Aspirin-Induced [MESH:D055963] (1055)
Hypersensitivity, Delayed [MESH:D006968] (3408)	Dermatitis, Allergic Contact [MESH:D017449] (3241)
Hypersensitivity, Immediate [MESH:D006969] (4980)	Asthma, Aspirin-Induced [MESH:D055963] (1055)
	Dermatitis, Atopic [MESH:D003876] (2052)
Respiratory Hypersensitivity [MESH:D012130] (4250)	Asthma [MESH:D001249] (3914)
Immunologic Deficiency Syndromes [MESH:D007153] (3788)
HIV Infections [MESH:D015658] (3402)	HIV Wasting Syndrome [MESH:D019247] (1956)
Immunoproliferative Disorders [MESH:D007160] (4761)
Lymphoproliferative Disorders [MESH:D008232] (4734)	Giant Lymph Node Hyperplasia [MESH:D005871] (1013)
	Multiple Myeloma [MESH:D009101] (2767)
Leukemia, Lymphoid [MESH:D007945] (3047)	Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754)
Leukemia, B-Cell [MESH:D015448] (2564)	Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562)
Lymphoma [MESH:D008223] (3684)
Lymphoma, Non-Hodgkin [MESH:D008228] (3330)	Burkitt Lymphoma [MESH:D002051] (691)
Lymphoma, B-Cell [MESH:D016393] (2624)	Burkitt Lymphoma [MESH:D002051] (691)
	Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012)
Paraproteinemias [MESH:D010265] (2791)	Multiple Myeloma [MESH:D009101] (2765)
C22. Animal Diseases	C22. Animal Diseases
Animal Diseases [MESH:D000820] (3656)	Disease Models, Animal [MESH:D004195] (2058)
	Mammary Neoplasms, Animal [MESH:D015674] (2735)
C23. Pathological Conditions, Signs and Symptoms	C23. Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical [MESH:D020763] (6074)	Alopecia [MESH:D000505] (1383)
Agenesis of Corpus Callosum [MESH:D061085] (197)	Donnai-Barrow syndrome [MESH:C536390] (40)
Calculi [MESH:D002137] (756)	Gallstones [MESH:D042882] (350)
Hernia [MESH:D006547] (2825)
Hernia, Diaphragmatic [MESH:D006548] (2647)	Congenital diaphragmatic hernia [MESH:C538080] (381)
Hypertrophy [MESH:D006984] (4476)
Cardiomegaly [MESH:D006332] (3802)	Hypertrophy, Left Ventricular [MESH:D017379] (1430)
Leukoplakia [MESH:D007971] (922)	Leukoplakia, Oral [MESH:D007972] (921)
Polyps [MESH:D011127] (1633)	Intestinal Polyps [MESH:D007417] (1592)
Pathologic Processes [MESH:D010335] (9863)	Arrhythmias, Cardiac [MESH:D001145] (4658)
	Hyperplasia [MESH:D006965] (2463)
	Ischemia [MESH:D007511] (3049)
	Necrosis [MESH:D009336] (4019)
	Neointima [MESH:D058426] (814)
	Nerve Degeneration [MESH:D009410] (4061)
Chromosome Aberrations [MESH:D002869] (2352)	Micronuclei, Chromosome-Defective [MESH:D048629] (1013)
Death [MESH:D003643] (1328)	Embryo Loss [MESH:D020964] (288)
Disease Attributes [MESH:D020969] (3654)	Disease Progression [MESH:D018450] (2868)
	Recurrence [MESH:D012008] (830)
Fibrosis [MESH:D005355] (3133)
Cicatrix [MESH:D002921] (1115)	Keloid [MESH:D007627] (1110)
Hemorrhage [MESH:D006470] (4451)	Shock, Hemorrhagic [MESH:D012771] (2042)
Intracranial Hemorrhages [MESH:D020300] (3241)	Cerebral Hemorrhage [MESH:D002543] (2872)
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)	Amenorrhea [MESH:D000568] (817)
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)
Shock [MESH:D012769] (2550)	Shock, Hemorrhagic [MESH:D012771] (2042)
Signs and Symptoms [MESH:D012816] (10659)	Edema [MESH:D004487] (3726)
Body Temperature Changes [MESH:D001832] (3130)	Fever [MESH:D005334] (2856)
Body Weight [MESH:D001835] (4972)	Fetal Weight [MESH:D020567] (12)
Body Weight Changes [MESH:D001836] (3206)	Weight Gain [MESH:D015430] (2595)
Weight Loss [MESH:D015431] (2512)
Emaciation [MESH:D004614] (2285)	Cachexia [MESH:D002100] (2283)
Overweight [MESH:D050177] (4455)	Obesity [MESH:D009765] (4454)
Neurologic Manifestations [MESH:D009461] (8702)	Seizures [MESH:D012640] (4502)
Dyskinesias [MESH:D020820] (3285)	Mental Retardation, X-Linked, Syndromic 10 [MESH:C564560] (54)
	Dystonia [MESH:D004421] (848)
	Hypokinesia [MESH:D018476] (279)
Neurobehavioral Manifestations [MESH:D019954] (4706)	Intellectual Disability [MESH:D008607] (1476)
Communication Disorders [MESH:D003147] (2918)	Learning Disorders [MESH:D007859] (2727)
Memory Disorders [MESH:D008569] (3233)	Amnesia [MESH:D000647] (1911)
Neuromuscular Manifestations [MESH:D020879] (2130)
Muscle Hypertonia [MESH:D009122] (775)	Muscle Rigidity [MESH:D009127] (617)
Pain [MESH:D010146] (3869)	Headache [MESH:D006261] (1417)
Paralysis [MESH:D010243] (2298)
Ophthalmoplegia [MESH:D009886] (1468)	Supranuclear Palsy, Progressive [MESH:D013494] (235)
Sensation Disorders [MESH:D012678] (5009)
Hearing Disorders [MESH:D006311] (2101)
Hearing Loss [MESH:D034381] (2066)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)
Hearing Loss, Sensorineural [MESH:D006319] (1227)	Donnai-Barrow syndrome [MESH:C536390] (40)
Somatosensory Disorders [MESH:D020886] (4000)	Hyperalgesia [MESH:D006930] (3929)
Pain [MESH:D010146] (4511)	Headache [MESH:D006261] (1417)
Chest Pain [MESH:D002637] (2642)
Angina Pectoris [MESH:D000787] (2568)	Acute Coronary Syndrome [MESH:D054058] (2286)
Signs and Symptoms, Respiratory [MESH:D012818] (2724)	Anoxia [MESH:D000860] (1698)
Urological Manifestations [MESH:D020924] (3532)
Proteinuria [MESH:D011507] (3293)	Donnai-Barrow syndrome [MESH:C536390] (40)
	Albuminuria [MESH:D000419] (2394)
C24. Occupational Diseases	C24. Occupational Diseases
Occupational Diseases [MESH:D009784] (3402)
Pneumoconiosis [MESH:D011009] (2670)	Berylliosis [MESH:D001607] (2005)
C25. Chemically-Induced Disorders	C25. Chemically-Induced Disorders
Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)	Drug-Induced Liver Injury [MESH:D056486] (4936)
	Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Drug Hypersensitivity [MESH:D004342] (4001)	Asthma, Aspirin-Induced [MESH:D055963] (1055)
Poisoning [MESH:D011041] (6703)	Arsenic Poisoning [MESH:D020261] (2540)
	Cadmium Poisoning [MESH:D002105] (180)
	Carbon Tetrachloride Poisoning [MESH:D002252] (102)
	Drug-Induced Liver Injury [MESH:D056486] (4936)
Neurotoxicity Syndromes [MESH:D020258] (3323)	Dyskinesia, Drug-Induced [MESH:D004409] (1389)
Substance-Related Disorders [MESH:D019966] (6308)	Amphetamine-Related Disorders [MESH:D019969] (2858)
	Cocaine-Related Disorders [MESH:D019970] (3054)
	Marijuana Abuse [MESH:D002189] (1132)
	Phencyclidine Abuse [MESH:D010623] (288)
Alcohol-Related Disorders [MESH:D019973] (3869)	Alcoholism [MESH:D000437] (1519)
Alcohol-Induced Disorders [MESH:D020751] (3350)
Liver Diseases, Alcoholic [MESH:D008108] (3243)	Liver Cirrhosis, Alcoholic [MESH:D008104] (3066)
C26. Wounds and Injuries	C26. Wounds and Injuries
Z. Exceptions (2454)	Not Fully Specified [NFS] (2454)
Wounds and Injuries [MESH:D014947] (5171)	Burns [MESH:D002056] (2565)
Craniocerebral Trauma [MESH:D006259] (3523)	Brain Injuries [MESH:D001930] (3431)
Spinal Cord Injuries [MESH:D013119] (2688)	Spinal Cord Compression [MESH:D013117] (1800)
Thoracic Injuries [MESH:D013898] (1831)	Lung Injury [MESH:D055370] (1814)
Trauma, Nervous System [MESH:D020196] (3535)
Craniocerebral Trauma [MESH:D006259] (3507)	Brain Injuries [MESH:D001930] (3431)
D02. Organic Chemicals	D02. Organic Chemicals
Organic Chemicals [MESH:D009930] (75987)
Hydrocarbons [MESH:D006838] (35762)
Hydrocarbons, Cyclic [MESH:D006844] (22983)
Hydrocarbons, Aromatic [MESH:D006841] (19108)	Benzene Derivatives [MESH:D001555] (10684)
F. Psychiatry and Psychology	F. Psychiatry and Psychology
Mental Disorders [MESH:D001523] (2063)
Delirium, Dementia, Amnestic, Cognitive Disorders [MESH:D019965] (487)
Dementia [MESH:D003704] (471)
Frontotemporal Lobar Degeneration [MESH:D057174] (112)
Frontotemporal Dementia [MESH:D057180] (109)	Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia [MESH:C563476] (57)
Mental Disorders Diagnosed in Childhood [MESH:D019952] (1245)
Developmental Disabilities [MESH:D002658] (151)	Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay [MESH:C567769] (22)