User:Byrial/Mesh ID
Made from a database dump from 2013-06-23.
Mysql query: /* __PRINT_QUERY__ */ SELECT s_item, s_string_value, s_datatype, (SELECT l_text FROM label WHERE l_id = s_item AND l_lang = 'en') FROM statement WHERE s_property = 486 ORDER BY s_string_value
Items with MeSH descriptor ID (P486) edit
- Q1598365 (Heparin-induced thrombocytopenia) MeSH ID = novalue
- Q3377653 (Scapular fracture) MeSH ID = novalue
- Q7796109 (Thoracic aorta injury) MeSH ID = somevalue
- Q5113996 (Chronic recurrent multifocal osteomyelitis) MeSH ID = C535456
- Q5656137 (Harding ataxia) MeSH ID = C535633
- Q3961699 (De Barsy syndrome) MeSH ID = C535990
- Q7267327 (Qazi–Markouizos syndrome) MeSH ID = C536259
- Q1958739 (Persistent Müllerian duct syndrome) MeSH ID = C536665
- Q4795508 (Aromatase excess syndrome) MeSH ID = C537436
- Q6837318 (Michels Caskey syndrome) MeSH ID = C537576
- Q4634217 (3-hydroxy-3-methylglutaryl-CoA lyase deficiency) MeSH ID = C538324
- Q319812 (Abetalipoproteinemia) MeSH ID = D000012
- Q164655 (Abscess) MeSH ID = D000038
- Q415833 (Acanthosis nigricans) MeSH ID = D000052
- Q340594 (achondroplasia) MeSH ID = D000130
- Q1516211 (Renal tubular acidosis) MeSH ID = D000141
- Q79928 (Acne) MeSH ID = D000152
- Q12199 (AIDS) MeSH ID = D000163
- Q618246 (Apert syndrome) MeSH ID = D000168
- Q189580 (Acromegaly) MeSH ID = D000172
- Q2300699 (Warthin's tumor) MeSH ID = D000235
- Q1615557 (Adiposis dolorosa) MeSH ID = D000274
- Q558070 (Pelvic inflammatory disease) MeSH ID = D000292
- Q366868 (Congenital adrenal hyperplasia) MeSH ID = D000312
- Q366964 (Adrenoleukodystrophy) MeSH ID = D000326
- Q5160407 (Congenital afibrinogenemia) MeSH ID = D000347
- Q332154 (Penuaan) MeSH ID = D000375
- Q174589 (Agoraphobia) MeSH ID = D000379
- Q584560 (dysgraphia) MeSH ID = D000381
- Q2161046 (Ainhum) MeSH ID = D000387
- Q857300 (?) MeSH ID = D000402
- Q81867 (albinism) MeSH ID = D000417
- Q209647 (Delirium tremens) MeSH ID = D000430
- Q205972 (Drunkenness) MeSH ID = D000435
- Q15326 (alcoholism) MeSH ID = D000437
- Q651680 (Alkaptonuria) MeSH ID = D000474
- Q5075435 (Alopecia areata) MeSH ID = D000506
- Q11081 (Alzheimer's disease) MeSH ID = D000544
- Q5326566 (Early-onset Alzheimer's disease) MeSH ID = D000544
- Q473753 (amniotic band syndrome) MeSH ID = D000652
- Q5164383 (Constriction Ring Syndrome) MeSH ID = D000652
- Q477415 (Amputation) MeSH ID = D000673
- Q206901 (amyotrophic lateral sclerosis) MeSH ID = D000690
- Q3045238 (Congenital insensitivity to pain) MeSH ID = D000699
- Q846316 (aplastic anemia) MeSH ID = D000741
- Q2610084 (Sideroblastic anemia) MeSH ID = D000756
- Q615645 (Fabry disease) MeSH ID = D000795
- Q1129007 (Angioedema) MeSH ID = D000799
- Q131749 (anorexia nervosa) MeSH ID = D000856
- Q129104 (anthrax) MeSH ID = D000881
- Q484631 (Imperforate anus) MeSH ID = D001006
- Q101004 (Aorta) MeSH ID = D001011
- Q616003 (Aortic aneurysm) MeSH ID = D001014
- Q616066 (Coarctation of the aorta) MeSH ID = D001017
- Q558623 (Aphakia) MeSH ID = D001035
- Q923164 (Expressive aphasia) MeSH ID = D001039
- Q1741331 (Receptive aphasia) MeSH ID = D001041
- Q373822 (eating disorder) MeSH ID = D001068
- Q120136 (Arcus senilis) MeSH ID = D001112
- Q1071707 (Arnold–Chiari malformation) MeSH ID = D001139
- Q184559 (arteriosclerosis) MeSH ID = D001161
- Q1584110 (Arteriovenous malformation) MeSH ID = D001165
- Q170990 (arthritis) MeSH ID = D001168
- Q861224 (juvenile idiopathic arthritis) MeSH ID = D001171
- Q187255 (rheumatoid arthritis) MeSH ID = D001172
- Q708165 (Arthrogryposis) MeSH ID = D001176
- Q842428 (Ascariasis) MeSH ID = D001196
- Q1430844 (Allergic bronchopulmonary aspergillosis) MeSH ID = D001229
- Q35869 (asthma) MeSH ID = D001249
- Q387082 (Ataxia telangiectasia) MeSH ID = D001260
- Q181923 (Attention-deficit hyperactivity disorder) MeSH ID = D001289
- Q38404 (autism) MeSH ID = D001321
- Q192360 (Autoimmunity) MeSH ID = D001327
- Q8084905 (autoimmune disease) MeSH ID = D001327
- Q805030 (Danubian endemic familial nephropathy) MeSH ID = D001449
- Q808892 (Barrett's esophagus) MeSH ID = D001471
- Q790971 (Bartter syndrome) MeSH ID = D001477
- Q12135 (mental disorder) MeSH ID = D001523
- Q911427 (Behçet's disease) MeSH ID = D001528
- Q822228 (Bernard–Soulier syndrome) MeSH ID = D001606
- Q131755 (bipolar disorder) MeSH ID = D001714
- Q185935 (Mania) MeSH ID = D001714
- Q1585769 (Urolithiasis) MeSH ID = D001744
- Q3825881 (Bladder stone) MeSH ID = D001744
- Q504775 (bladder cancer) MeSH ID = D001749
- Q1469646 (Bloom syndrome) MeSH ID = D001816
- Q141440 (Brain abscess) MeSH ID = D001922
- Q1995526 (Traumatic brain injury) MeSH ID = D001930
- Q5463841 (Focal and diffuse brain injury) MeSH ID = D001930
- Q233309 (brain tumor) MeSH ID = D001932
- Q128581 (breast cancer) MeSH ID = D001943
- Q6742919 (Male breast cancer) MeSH ID = D001943
- Q173022 (bronchitis) MeSH ID = D001991
- Q1900400 (Acute bronchitis) MeSH ID = D001991
- Q922640 (Bronchopulmonary dysplasia) MeSH ID = D001997
- Q1016605 (Burkitt's lymphoma) MeSH ID = D002051
- Q273510 (Candidiasis) MeSH ID = D002177
- Q3705799 (Chronic mucocutaneous candidiasis) MeSH ID = D002178
- Q1734755 (Carcinoid) MeSH ID = D002276
- Q809758 (Basal-cell carcinoma) MeSH ID = D002280
- Q47912 (lung cancer) MeSH ID = D002283
- Q681817 (squamous-cell carcinoma) MeSH ID = D002294
- Q283656 (Dilated cardiomyopathy) MeSH ID = D002311
- Q1364270 (Hypertrophic cardiomyopathy) MeSH ID = D002312
- Q332293 (Carpal tunnel syndrome) MeSH ID = D002349
- Q1623043 (Tinel sign) MeSH ID = D002349
- Q944473 (Cataplexy) MeSH ID = D002385
- Q501571 (Catatonia) MeSH ID = D002389
- Q11088 (coeliac disease) MeSH ID = D002446
- Q3961686 (Ramsay Hunt syndrome type I) MeSH ID = D002527
- Q6058359 (Intracranial berry aneurysm) MeSH ID = D002532
- Q191570 (Cerebral arteriovenous malformation) MeSH ID = D002538
- Q593958 (Transient ischemic attack) MeSH ID = D002546
- Q210427 (Cerebral palsy) MeSH ID = D002547
- Q4813631 (Athetoid cerebral palsy) MeSH ID = D002547
- Q2028015 (Alpers' disease) MeSH ID = D002549
- Q2909420 (Diffuse myelinoclastic sclerosis) MeSH ID = D002549
- Q160105 (cervical cancer) MeSH ID = D002583
- Q934034 (Chédiak–Higashi syndrome) MeSH ID = D002609
- Q568865 (Cherubism) MeSH ID = D002636
- Q1142806 (Developmental disability) MeSH ID = D002658
- Q153356 (Chlamydia infection) MeSH ID = D002690
- Q12090 (cholera) MeSH ID = D002771
- Q559082 (Chondrocalcinosis) MeSH ID = D002805
- Q1076087 (Chondrosarcoma) MeSH ID = D002813
- Q1076389 (Chordoma) MeSH ID = D002817
- Q1076421 (chorea) MeSH ID = D002819
- Q2562598 (Haemophilia B) MeSH ID = D002836
- Q1690779 (Primary ciliary dyskinesia) MeSH ID = D002925
- Q781618 (Cleidocranial dysostosis) MeSH ID = D002973
- Q1162164 (club foot) MeSH ID = D003025
- Q868137 (Coccidioidomycosis) MeSH ID = D003047
- Q914389 (Cockayne syndrome) MeSH ID = D003057
- Q1477 (ulcerative colitis) MeSH ID = D003093
- Q3924862 (Intestinal pseudoobstruction) MeSH ID = D003112
- Q133696 (color blindness) MeSH ID = D003117
- Q783644 (Hereditary nonpolyposis colorectal cancer) MeSH ID = D003123
- Q12125 (Common cold) MeSH ID = D003139
- Q131736 (infectious disease) MeSH ID = D003141
- Q167844 (conjunctivitis) MeSH ID = D003231
- Q844935 (Coronary artery disease) MeSH ID = D003324
- Q779250 (Crouzon syndrome) MeSH ID = D003394
- Q378183 (Craniosynostosis) MeSH ID = D003398
- Q1140000 (Crigler–Najjar syndrome) MeSH ID = D003414
- Q1472 (Crohn's disease) MeSH ID = D003424
- Q966052 (Cryptorchidism) MeSH ID = D003456
- Q2735907 (Cutis laxa) MeSH ID = D003483
- Q245590 (Cyclothymia) MeSH ID = D003527
- Q178194 (cystic fibrosis) MeSH ID = D003550
- Q1149046 (Cystinuria) MeSH ID = D003555
- Q6929 (Human cytomegalovirus) MeSH ID = D003586
- Q6946 (Cytomegalovirus) MeSH ID = D003586
- Q733493 (Dandy–Walker syndrome) MeSH ID = D003616
- Q189643 (Delusion) MeSH ID = D003702
- Q18579 (Frontotemporal lobar degeneration) MeSH ID = D003704
- Q320719 (Dependent personality disorder) MeSH ID = D003859
- Q2338307 (Depersonalization disorder) MeSH ID = D003861
- Q42844 (clinical depression) MeSH ID = D003865
- Q268667 (Atopic dermatitis) MeSH ID = D003876
- Q220551 (Diabetes insipidus) MeSH ID = D003919
- Q124407 (diabetes mellitus type 1) MeSH ID = D003922
- Q6556681 (Lipoatrophic diabetes) MeSH ID = D003923
- Q663041 (Maturity onset diabetes of the young) MeSH ID = D003924
- Q3025883 (diabetes mellitus type 2) MeSH ID = D003924
- Q777717 (Diabetic coma) MeSH ID = D003926
- Q498487 (Camurati–Engelmann disease) MeSH ID = D003966
- Q5274956 (Dientamoebiasis) MeSH ID = D004030
- Q525642 (DiGeorge syndrome) MeSH ID = D004062
- Q278158 (Diverticulosis) MeSH ID = D004240
- Q361648 (Double outlet right ventricle) MeSH ID = D004310
- Q7688951 (Taussig–Bing syndrome) MeSH ID = D004310
- Q47715 (Down syndrome) MeSH ID = D004314
- Q5302758 (Down's Syndrome Scotland) MeSH ID = D004314
- Q1262684 (Duane syndrome) MeSH ID = D004370
- Q1330254 (Dupuytren's contracture) MeSH ID = D004387
- Q369262 (Growth hormone deficiency) MeSH ID = D004393
- Q225957 (Dysarthria) MeSH ID = D004401
- Q2325854 (Familial dysautonomia) MeSH ID = D004402
- Q132971 (dyslexia) MeSH ID = D004410
- Q1269320 (Dysplastic nevus) MeSH ID = D004416
- Q906492 (Dystonia) MeSH ID = D004421
- Q656199 (Torsion dystonia) MeSH ID = D004422
- Q5325633 (Ear disease) MeSH ID = D004427
- Q277452 (Ebstein's anomaly) MeSH ID = D004437
- Q1827028 (Ectopia lentis) MeSH ID = D004479
- Q988594 (Eczema) MeSH ID = D004485
- Q2298020 (Hereditary elliptocytosis) MeSH ID = D004612
- Q3358864 (Southeast Asian ovalocytosis) MeSH ID = D004612
- Q1332448 (Ellis–van Creveld syndrome) MeSH ID = D004613
- Q199615 (Encephalitis) MeSH ID = D004660
- Q424242 (Acute disseminated encephalomyelitis) MeSH ID = D004673
- Q1419261 (Maffucci syndrome) MeSH ID = D004687
- Q2388598 (Ollier disease) MeSH ID = D004687
- Q82504 (Endocarditis) MeSH ID = D004696
- Q205764 (Endometriosis) MeSH ID = D004715
- Q2012569 (Adenomyosis) MeSH ID = D004715
- Q379476 (Epidermoid cyst) MeSH ID = D004814
- Q1878682 (Toxic epidermal necrolysis) MeSH ID = D004816
- Q974691 (Epidermodysplasia verruciformis) MeSH ID = D004819
- Q41571 (epilepsy) MeSH ID = D004827
- Q616667 (temporal lobe epilepsy) MeSH ID = D004833
- Q1363738 (Erythema nodosum) MeSH ID = D004893
- Q3843804 (Acute erythroid leukemia) MeSH ID = D004915
- Q524353 (Erythromelalgia) MeSH ID = D004916
- Q372701 (esophageal cancer) MeSH ID = D004938
- Q298230 (Esophagitis) MeSH ID = D004941
- Q1952467 (Hereditary multiple exostoses) MeSH ID = D005097
- Q250365 (Parry–Romberg syndrome) MeSH ID = D005150
- Q2686385 (Factitious disorder) MeSH ID = D005162
- Q4135181 (Haemophilia C) MeSH ID = D005173
- Q1393725 (Factor XIII deficiency) MeSH ID = D005177
- Q845779 (Fanconi anemia) MeSH ID = D005199
- Q1404470 (Felty's syndrome) MeSH ID = D005258
- Q400277 (Fetal alcohol syndrome) MeSH ID = D005310
- Q688949 (Fibromuscular dysplasia) MeSH ID = D005352
- Q727008 (McCune–Albright syndrome) MeSH ID = D005359
- Q5463847 (Focal dermal hypoplasia) MeSH ID = D005489
- Q769815 (Food allergy) MeSH ID = D005512
- Q221472 (Fragile X syndrome) MeSH ID = D005600
- Q913856 (Friedreich's ataxia) MeSH ID = D005621
- Q1609755 (Hereditary fructose intolerance) MeSH ID = D005633
- Q1464888 (Fuchs' dystrophy) MeSH ID = D005642
- Q177878 (Fucosidosis) MeSH ID = D005645
- Q431168 (Pectus excavatum) MeSH ID = D005660
- Q5517832 (Galactose-1-phosphate uridylyltransferase deficiency) MeSH ID = D005693
- Q5518905 (Gallbladder disease) MeSH ID = D005705
- Q1702335 (Gardner's syndrome) MeSH ID = D005736
- Q975705 (Ménétrier's disease) MeSH ID = D005758
- Q223591 (Gastroesophageal reflux disease) MeSH ID = D005764
- Q861645 (Gaucher's disease) MeSH ID = D005776
- Q1049021 (Gender identity disorder) MeSH ID = D005783
- Q752216 (Gilbert's syndrome) MeSH ID = D005878
- Q191779 (Tourette syndrome) MeSH ID = D005879
- Q282142 (Glioblastoma multiforme) MeSH ID = D005909
- Q4139987 (Glomus tumor) MeSH ID = D005918
- Q1146454 (IgA nephropathy) MeSH ID = D005922
- Q1435223 (Focal segmental glomerulosclerosis) MeSH ID = D005923
- Q848343 (Glucose-6-phosphate dehydrogenase deficiency) MeSH ID = D005955
- Q1365789 (Glycogen storage disease type II) MeSH ID = D006009
- Q494922 (Glycogen storage disease type III) MeSH ID = D006010
- Q829150 (Glycogen storage disease type IV) MeSH ID = D006011
- Q787751 (Glycogen storage disease type V) MeSH ID = D006012
- Q1947298 (Glycogen storage disease type VI) MeSH ID = D006013
- Q1251847 (Phosphofructokinase deficiency) MeSH ID = D006014
- Q1207967 (Renal glycosuria) MeSH ID = D006030
- Q165135 (goiter) MeSH ID = D006042
- Q769988 (Goldenhar syndrome) MeSH ID = D006053
- Q957751 (XY gonadal dysgenesis) MeSH ID = D006061
- Q133087 (gout) MeSH ID = D006073
- Q1765748 (Transplant rejection) MeSH ID = D006084
- Q1194520 (Graft-versus-host disease) MeSH ID = D006086
- Q2165663 (Chronic granulomatous disease) MeSH ID = D006105
- Q16483 (Graves' disease) MeSH ID = D006111
- Q1459851 (Hallermann–Streiff syndrome) MeSH ID = D006210
- Q1436162 (Pantothenate kinase-associated neurodegeneration) MeSH ID = D006211
- Q130741 (Hallucination) MeSH ID = D006212
- Q474254 (Bannayan–Riley–Ruvalcaba syndrome) MeSH ID = D006223
- Q200985 (Hartnup disease) MeSH ID = D006250
- Q2920572 (Head injury) MeSH ID = D006259
- Q181754 (heart failure) MeSH ID = D006333
- Q7316745 (Retiform hemangioendothelioma) MeSH ID = D006390
- Q2716919 (Epidural hematoma) MeSH ID = D006407
- Q1479494 (Paroxysmal nocturnal hemoglobinuria) MeSH ID = D006457
- Q162266 (Hemolytic-uremic syndrome) MeSH ID = D006463
- Q642548 (Hepatic encephalopathy) MeSH ID = D006501
- Q183098 (Budd–Chiari syndrome) MeSH ID = D006502
- Q5731687 (Hepatic veno-occlusive disease) MeSH ID = D006504
- Q131742 (hepatitis) MeSH ID = D006505
- Q157661 (Hepatitis A) MeSH ID = D006506
- Q6853 (hepatitis B) MeSH ID = D006509
- Q154869 (Hepatitis C) MeSH ID = D006526
- Q117121 (Wilson's disease) MeSH ID = D006527
- Q1148337 (hepatocellular carcinoma) MeSH ID = D006528
- Q2163245 (Congenital diaphragmatic hernia) MeSH ID = D006548
- Q727153 (Hiatus hernia) MeSH ID = D006551
- Q1521567 (Omphalocele) MeSH ID = D006554
- Q625935 (Hip dysplasia) MeSH ID = D006618
- Q634638 (Dislocation of hip) MeSH ID = D006618
- Q1343645 (Hirschsprung's disease) MeSH ID = D006627
- Q374036 (Langerhans cell histiocytosis) MeSH ID = D006646
- Q6533637 (Letterer–Siwe disease) MeSH ID = D006646
- Q994859 (Homocystinuria) MeSH ID = D006712
- Q1126839 (Horner's syndrome) MeSH ID = D006732
- Q190564 (Huntington's disease) MeSH ID = D006816
- Q881855 (Hydatidiform mole) MeSH ID = D006828
- Q1640860 (Hyperaldosteronism) MeSH ID = D006929
- Q1512812 (Rotor syndrome) MeSH ID = D006933
- Q2711291 (familial hypercholesterolemia) MeSH ID = D006938
- Q1079120 (Hyperlipidemia) MeSH ID = D006949
- Q3801522 (Infantile cortical hyperostosis) MeSH ID = D006958
- Q1344835 (Hyperparathyroidism) MeSH ID = D006961
- Q42982 (Allergy) MeSH ID = D006967
- Q1641128 (Hypertelorism) MeSH ID = D006972
- Q41861 (hypertension) MeSH ID = D006973
- Q16499 (Hyperthyroidism) MeSH ID = D006980
- Q5958740 (Hyperthyroxinemia) MeSH ID = D006981
- Q595010 (Hypertrichosis) MeSH ID = D006983
- Q202758 (Hypoglycemia) MeSH ID = D007003
- Q938107 (Hypogonadism) MeSH ID = D007006
- Q1586088 (Hypoparathyroidism) MeSH ID = D007011
- Q1313510 (Hypophosphatasia) MeSH ID = D007014
- Q922411 (hypopituitarism) MeSH ID = D007018
- Q184674 (Erectile dysfunction) MeSH ID = D007172
- Q959457 (Syndrome of inappropriate antidiuretic hormone secretion) MeSH ID = D007177
- Q884590 (Incontinentia pigmenti) MeSH ID = D007184
- Q2840 (influenza) MeSH ID = D007251
- Q697117 (Spinal disc herniation) MeSH ID = D007405
- Q1424612 (Intussusception) MeSH ID = D007443
- Q49989 (Creutzfeldt–Jakob disease) MeSH ID = D007562
- Q1263039 (Dubin–Johnson syndrome) MeSH ID = D007566
- Q2336873 (Hyperimmunoglobulin E syndrome) MeSH ID = D007589
- Q1641042 (hypermobility) MeSH ID = D007593
- Q2605012 (Kearns–Sayre syndrome) MeSH ID = D007625
- Q580506 (Darier's disease) MeSH ID = D007644
- Q4675784 (Acrokeratosis verruciformis) MeSH ID = D007644
- Q7128426 (Palmoplantar keratoderma) MeSH ID = D007645
- Q178623 (Kidney stone) MeSH ID = D007669
- Q736715 (Chronic kidney disease) MeSH ID = D007676
- Q639203 (Menkes disease) MeSH ID = D007706
- Q1774751 (Klippel–Feil syndrome) MeSH ID = D007714
- Q1774750 (Klippel–Trénaunay–Weber syndrome) MeSH ID = D007715
- Q274615 (Kuru) MeSH ID = D007729
- Q213151 (Kwashiorkor) MeSH ID = D007732
- Q1432397 (Kyasanur forest disease) MeSH ID = D007733
- Q219223 (Lactose intolerance) MeSH ID = D007787
- Q706845 (Lassa fever) MeSH ID = D007835
- Q3961678 (Laurence–Moon syndrome) MeSH ID = D007849
- Q110315 (Lead poisoning) MeSH ID = D007855
- Q3441028 (Lecithin cholesterol acyltransferase deficiency) MeSH ID = D007863
- Q1456403 (Legg–Calvé–Perthes syndrome) MeSH ID = D007873
- Q1815019 (Leigh's disease) MeSH ID = D007888
- Q556281 (uterine fibroid) MeSH ID = D007889
- Q331283 (Leishmaniasis) MeSH ID = D007896
- Q36956 (leprosy) MeSH ID = D007918
- Q727436 (Lesch–Nyhan syndrome) MeSH ID = D007926
- Q29496 (leukemia) MeSH ID = D007938
- Q7201765 (Plasma cell leukemia) MeSH ID = D007952
- Q511372 (Krabbe disease) MeSH ID = D007965
- Q1120682 (Metachromatic leukodystrophy) MeSH ID = D007966
- Q704930 (Progressive multifocal leukoencephalopathy) MeSH ID = D007968
- Q2722350 (Hurler syndrome) MeSH ID = D008059
- Q653078 (Whipple's disease) MeSH ID = D008061
- Q2500124 (Urbach–Wiethe disease) MeSH ID = D008065
- Q1691351 (Lipomatosis) MeSH ID = D008068
- Q4887975 (Benign symmetric lipomatosis) MeSH ID = D008069
- Q2349695 (Lipoprotein lipase deficiency) MeSH ID = D008072
- Q1072420 (primary biliary cirrhosis) MeSH ID = D008105
- Q1760607 (Loa loa filariasis) MeSH ID = D008118
- Q1758283 (Lown–Ganong–Levine syndrome) MeSH ID = D008151
- Q1485 (systemic lupus erythematosus) MeSH ID = D008180
- Q201989 (Lyme disease) MeSH ID = D008193
- Q916398 (Lymphedema) MeSH ID = D008209
- Q6860732 (Milroy's disease) MeSH ID = D008209
- Q123251 (follicular lymphoma) MeSH ID = D008224
- Q1138590 (Non-Hodgkin lymphoma) MeSH ID = D008228
- Q8041558 (X-linked lymphoproliferative disease) MeSH ID = D008232
- Q1778287 (Waldenström's macroglobulinemia) MeSH ID = D008258
- Q524095 (Macroglossia) MeSH ID = D008260
- Q830308 (macular degeneration) MeSH ID = D008268
- Q12156 (malaria) MeSH ID = D008288
- Q1585081 (Malignant hyperthermia) MeSH ID = D008305
- Q488231 (Malingering) MeSH ID = D008306
- Q744790 (Treacher Collins syndrome) MeSH ID = D008342
- Q250449 (Alpha-mannosidosis) MeSH ID = D008363
- Q402575 (Maple syrup urine disease) MeSH ID = D008375
- Q208562 (Marfan syndrome) MeSH ID = D008382
- Q112670 (Mastocytosis) MeSH ID = D008415
- Q79793 (measles) MeSH ID = D008457
- Q388628 (Meckel's diverticulum) MeSH ID = D008467
- Q1918881 (Meconium aspiration syndrome) MeSH ID = D008471
- Q1333608 (Medulloblastoma) MeSH ID = D008527
- Q180614 (Melanoma) MeSH ID = D008545
- Q187882 (Freckle) MeSH ID = D008548
- Q1919487 (Melkersson–Rosenthal syndrome) MeSH ID = D008556
- Q1127727 (Melorheostosis) MeSH ID = D008557
- Q460167 (Ménière's disease) MeSH ID = D008575
- Q369157 (Meningioma) MeSH ID = D008579
- Q32069 (Meningism) MeSH ID = D008580
- Q48143 (Meningitis) MeSH ID = D008581
- Q6896359 (Mollaret's meningitis) MeSH ID = D008582
- Q1077603 (Mesothelioma) MeSH ID = D008654
- Q431643 (microcephaly) MeSH ID = D008831
- Q133823 (migraine) MeSH ID = D008881
- Q735652 (Mitral valve prolapse) MeSH ID = D008945
- Q2064603 (Pleomorphic adenoma) MeSH ID = D008949
- Q309067 (Motion sickness) MeSH ID = D009041
- Q1951267 (Moyamoya disease) MeSH ID = D009072
- Q265936 (Kawasaki disease) MeSH ID = D009080
- Q931538 (Mucolipidosis type IV) MeSH ID = D009081
- Q2200359 (Sanfilippo syndrome) MeSH ID = D009084
- Q580285 (Morquio syndrome) MeSH ID = D009085
- Q576109 (Maroteaux–Lamy syndrome) MeSH ID = D009087
- Q467635 (Multiple myeloma) MeSH ID = D009101
- Q8277 (multiple sclerosis) MeSH ID = D009103
- Q18657 (Dissociative identity disorder) MeSH ID = D009105
- Q7577466 (Spinal muscular atrophies) MeSH ID = D009134
- Q692536 (Myopathy) MeSH ID = D009135
- Q1137767 (Muscular dystrophy) MeSH ID = D009136
- Q8285 (Myasthenia gravis) MeSH ID = D009157
- Q1891209 (Mycosis fungoides) MeSH ID = D009182
- Q202217 (Transverse myelitis) MeSH ID = D009188
- Q847583 (cardiomyopathy) MeSH ID = D009202
- Q12152 (myocardial infarction) MeSH ID = D009203
- Q1433212 (Myositis) MeSH ID = D009220
- Q1410831 (Fibrodysplasia ossificans progressiva) MeSH ID = D009221
- Q1860507 (Myotonic dystrophy) MeSH ID = D009223
- Q587420 (Myotonia congenita) MeSH ID = D009224
- Q589612 (Myxoma) MeSH ID = D009232
- Q189561 (Narcolepsy) MeSH ID = D009290
- Q1693598 (nasopharyngeal carcinoma) MeSH ID = D009303
- Q12078 (cancer) MeSH ID = D009369
- Q1331116 (Alport syndrome) MeSH ID = D009394
- Q756289 (Wilms' tumor) MeSH ID = D009396
- Q548213 (Neural tube defect) MeSH ID = D009436
- Q510236 (Neurasthenia) MeSH ID = D009440
- Q938205 (Neuroblastoma) MeSH ID = D009447
- Q1112752 (Watson syndrome) MeSH ID = D009456
- Q7616509 (neurofibromatosis type I) MeSH ID = D009456
- Q1424956 (Neuroleptic malignant syndrome) MeSH ID = D009459
- Q1753778 (Batten disease) MeSH ID = D009472
- Q501694 (Congenital insensitivity to pain with anhidrosis) MeSH ID = D009477
- Q3702898 (Hereditary sensory and autonomic neuropathy) MeSH ID = D009477
- Q863857 (Halo nevus) MeSH ID = D009508
- Q1419931 (Niemann–Pick disease) MeSH ID = D009542
- Q3281285 (Niemann–Pick disease, SMPD1-associated) MeSH ID = D009542
- Q1543446 (Noonan syndrome) MeSH ID = D009634
- Q1200839 (Oculocerebrorenal syndrome) MeSH ID = D009800
- Q972514 (Optic neuritis) MeSH ID = D009902
- Q7103739 (Orofaciodigital syndrome 1) MeSH ID = D009958
- Q2035074 (Paget's disease of bone) MeSH ID = D010001
- Q799615 (Osteitis fibrosa cystica) MeSH ID = D010002
- Q62736 (Osteoarthritis) MeSH ID = D010003
- Q7243138 (Primary hypertrophic osteoathropathy) MeSH ID = D010004
- Q127556 (Osteochondritis dissecans) MeSH ID = D010008
- Q1452604 (Multiple epiphyseal dysplasia) MeSH ID = D010009
- Q1755568 (Osteopetrosis) MeSH ID = D010022
- Q1477777 (Osteopoikilosis) MeSH ID = D010023
- Q165328 (Osteoporosis) MeSH ID = D010024
- Q756610 (otosclerosis) MeSH ID = D010040
- Q212961 (pancreatic cancer) MeSH ID = D010190
- Q1527888 (Pancreatitis) MeSH ID = D010195
- Q6320789 (Papillon–Lefèvre syndrome) MeSH ID = D010214
- Q1399155 (Fazio-Londe disease) MeSH ID = D010244
- Q2060353 (Bulbar palsy) MeSH ID = D010244
- Q721073 (Delusional disorder) MeSH ID = D010259
- Q1229994 (Paranoia) MeSH ID = D010259
- Q178059 (Paraphilia) MeSH ID = D010262
- Q8388 (Pedophilia) MeSH ID = D010378
- Q975182 (Pelger-Huet anomaly) MeSH ID = D010381
- Q627291 (Cicatricial pemphigoid) MeSH ID = D010390
- Q1483214 (Pemphigus) MeSH ID = D010392
- Q874586 (Peyronie's disease) MeSH ID = D010411
- Q1144618 (Familial Mediterranean fever) MeSH ID = D010505
- Q1544989 (Peutz–Jeghers syndrome) MeSH ID = D010580
- Q1191062 (Phantom limb) MeSH ID = D010591
- Q194041 (phenylketonuria) MeSH ID = D010661
- Q5958471 (Hyperphenylalaninemia) MeSH ID = D010661
- Q536269 (pheochromocytoma) MeSH ID = D010673
- Q281928 (Social anxiety disorder) MeSH ID = D010698
- Q202394 (Obesity hypoventilation syndrome) MeSH ID = D010845
- Q1756040 (Pierre Robin syndrome) MeSH ID = D010855
- Q907921 (Incontinentia pigmenti achromians) MeSH ID = D010859
- Q991538 (?) MeSH ID = D010899
- Q766856 (Pityriasis rubra pilaris) MeSH ID = D010916
- Q1471410 (placenta praevia) MeSH ID = D010923
- Q133780 (plague) MeSH ID = D010930
- Q7202249 (Platelet storage pool deficiency) MeSH ID = D010981
- Q133125 (Pneumocystis pneumonia) MeSH ID = D011020
- Q203601 (Pneumothorax) MeSH ID = D011030
- Q1583485 (Rothmund–Thomson syndrome) MeSH ID = D011038
- Q633859 (Poland syndrome) MeSH ID = D011045
- Q500816 (Polycystic ovary syndrome) MeSH ID = D011085
- Q1369011 (Familial adenomatous polyposis) MeSH ID = D011125
- Q594013 (Prader–Willi syndrome) MeSH ID = D011218
- Q11995 (pregnancy) MeSH ID = D011247
- Q213098 (progeria) MeSH ID = D011371
- Q181257 (prostate cancer) MeSH ID = D011471
- Q372752 (Prostatitis) MeSH ID = D011472
- Q284070 (Protein losing enteropathy) MeSH ID = D011504
- Q250354 (Prune belly syndrome) MeSH ID = D011535
- Q200745 (Pseudohypoaldosteronism) MeSH ID = D011546
- Q819207 (Pseudohypoparathyroidism) MeSH ID = D011547
- Q1477265 (Pseudopseudohypoparathyroidism) MeSH ID = D011556
- Q741208 (Idiopathic intracranial hypertension) MeSH ID = D011559
- Q1052391 (Pseudoxanthoma elasticum) MeSH ID = D011561
- Q179945 (Psoriasis) MeSH ID = D011565
- Q3064951 (Psychomotor retardation) MeSH ID = D011596
- Q834047 (Schizoaffective disorder) MeSH ID = D011618
- Q2914688 (Schizophreniform disorder) MeSH ID = D011618
- Q1516012 (Delayed puberty) MeSH ID = D011628
- Q224513 (Precocious puberty) MeSH ID = D011629
- Q448698 (Pulmonary alveolar proteinosis) MeSH ID = D011649
- Q220570 (Pulmonary embolism) MeSH ID = D011655
- Q424258 (Acute interstitial pneumonitis) MeSH ID = D011658
- Q2290446 (Idiopathic pulmonary fibrosis) MeSH ID = D011658
- Q1426491 (Thrombotic thrombocytopenic purpura) MeSH ID = D011697
- Q506652 (Pyelonephritis) MeSH ID = D011704
- Q164818 (Q fever) MeSH ID = D011778
- Q1053824 (Raynaud's phenomenon) MeSH ID = D011928
- Q2062483 (Rectal prolapse) MeSH ID = D012005
- Q177809 (Refsum disease) MeSH ID = D012035
- Q877796 (Repetitive strain injury) MeSH ID = D012090
- Q754348 (Infant respiratory distress syndrome) MeSH ID = D012127
- Q916280 (Restless legs syndrome) MeSH ID = D012148
- Q847057 (Retinitis pigmentosa) MeSH ID = D012174
- Q500695 (retinoblastoma) MeSH ID = D012175
- Q1423087 (Retinopathy of prematurity) MeSH ID = D012178
- Q917069 (Rhabdomyolysis) MeSH ID = D012206
- Q1898141 (Rhabdomyosarcoma) MeSH ID = D012208
- Q183392 (Rickets) MeSH ID = D012279
- Q326638 (Rift Valley fever) MeSH ID = D012295
- Q666980 (Rubinstein–Taybi syndrome) MeSH ID = D012415
- Q917227 (Sandhoff disease) MeSH ID = D012497
- Q193894 (Sarcoidosis) MeSH ID = D012507
- Q1138580 (Ewing's sarcoma) MeSH ID = D012512
- Q725345 (Kaposi's sarcoma) MeSH ID = D012514
- Q549534 (osteosarcoma) MeSH ID = D012516
- Q167178 (scabies) MeSH ID = D012532
- Q1532790 (Scheuermann's disease) MeSH ID = D012544
- Q498237 (Schizoid personality disorder) MeSH ID = D012557
- Q267759 (Disorganized schizophrenia) MeSH ID = D012562
- Q861560 (Schizotypal personality disorder) MeSH ID = D012569
- Q5340515 (systemic scleroderma) MeSH ID = D012595
- Q163865 (scurvy) MeSH ID = D012614
- Q852376 (Seizure) MeSH ID = D012640
- Q6279182 (epileptic seizure) MeSH ID = D012640
- Q3959673 (Neurogenic shock) MeSH ID = D012769
- Q662272 (Short bowel syndrome) MeSH ID = D012778
- Q7507642 (Sickle cell trait) MeSH ID = D012805
- Q183344 (Sinusitis) MeSH ID = D012852
- Q1456383 (Situs inversus) MeSH ID = D012857
- Q335555 (Sjögren's syndrome) MeSH ID = D012859
- Q1971607 (Skull fracture) MeSH ID = D012887
- Q213600 (Sleep apnea) MeSH ID = D012891
- Q177190 (sleep disorder) MeSH ID = D012893
- Q1041258 (West syndrome) MeSH ID = D013036
- Q1434575 (Testicular torsion) MeSH ID = D013086
- Q541244 (Hereditary spherocytosis) MeSH ID = D013103
- Q1097028 (Spondylosis) MeSH ID = D013128
- Q2628677 (Marinesco–Sjögren syndrome) MeSH ID = D013132
- Q7578543 (Splenic infarction) MeSH ID = D013159
- Q52849 (Ankylosing spondylitis) MeSH ID = D013167
- Q973524 (Spondylolisthesis) MeSH ID = D013168
- Q585911 (Tropical sprue) MeSH ID = D013182
- Q1053948 (Stevens–Johnson syndrome) MeSH ID = D013262
- Q189588 (stomach cancer) MeSH ID = D013274
- Q179951 (Strabismus) MeSH ID = D013285
- Q2360849 (Strongyloidiasis) MeSH ID = D013322
- Q1886238 (Sturge–Weber syndrome) MeSH ID = D013341
- Q186676 (Stuttering) MeSH ID = D013342
- Q693442 (Subarachnoid hemorrhage) MeSH ID = D013345
- Q1412866 (Subcutaneous emphysema) MeSH ID = D013352
- Q161801 (Sudden infant death syndrome) MeSH ID = D013398
- Q945930 (Progressive supranuclear palsy) MeSH ID = D013494
- Q1360044 (syndactyly) MeSH ID = D013576
- Q2619315 (Synovial sarcoma) MeSH ID = D013584
- Q41083 (syphilis) MeSH ID = D013587
- Q1112977 (Syringomyelia) MeSH ID = D013595
- Q432462 (Takayasu's arteritis) MeSH ID = D013625
- Q1442621 (Tangier disease) MeSH ID = D013631
- Q560337 (Tay–Sachs disease) MeSH ID = D013661
- Q776881 (Hereditary hemorrhagic telangiectasia) MeSH ID = D013683
- Q707816 (Giant-cell arteritis) MeSH ID = D013700
- Q473262 (Complete androgen insensitivity syndrome) MeSH ID = D013734
- Q324464 (Testicular cancer) MeSH ID = D013736
- Q47790 (Tetanus) MeSH ID = D013742
- Q1126831 (Tetralogy of Fallot) MeSH ID = D013771
- Q1787020 (Thanatophoric dysplasia) MeSH ID = D013796
- Q1529258 (Glanzmann's thrombasthenia) MeSH ID = D013915
- Q1368780 (Essential thrombocytosis) MeSH ID = D013920
- Q585285 (Thrombocytopenia) MeSH ID = D013921
- Q502785 (Thyroglossal cyst) MeSH ID = D013955
- Q2292945 (Papillary thyroid cancer) MeSH ID = D013964
- Q7812743 (Toddler's fracture) MeSH ID = D013978
- Q2504473 (fissured tongue) MeSH ID = D014063
- Q4116448 (Laryngotracheal stenosis) MeSH ID = D014135
- Q7831318 (Tracheobronchomegaly) MeSH ID = D014137
- Q1758730 (Transposition of the great vessels) MeSH ID = D014188
- Q844903 (Trisomy) MeSH ID = D014314
- Q3055156 (Persistent truncus arteriosus) MeSH ID = D014339
- Q649558 (Chagas disease) MeSH ID = D014355
- Q12204 (tuberculosis) MeSH ID = D014376
- Q1362721 (Tuberous sclerosis) MeSH ID = D014402
- Q202849 (Turner syndrome) MeSH ID = D014424
- Q83319 (typhoid) MeSH ID = D014435
- Q1290616 (Epidemic typhus) MeSH ID = D014438
- Q1122485 (Urethritis) MeSH ID = D014526
- Q221668 (Urinary tract infection) MeSH ID = D014552
- Q1418513 (Uterine atony) MeSH ID = D014593
- Q356372 (Uveal melanoma) MeSH ID = D014604
- Q280027 (Uveitis) MeSH ID = D014605
- Q1986297 (Vaccinia) MeSH ID = D014615
- Q201180 (Varicose veins) MeSH ID = D014648
- Q817310 (Benign paroxysmal positional vertigo) MeSH ID = D014717
- Q10855957 (Hypovitaminosis D) MeSH ID = D014808
- Q180152 (Vitiligo) MeSH ID = D014820
- Q709360 (Von Willebrand disease) MeSH ID = D014842
- Q101971 (wart) MeSH ID = D014860
- Q1161568 (Wegener's granulomatosis) MeSH ID = D014890
- Q580290 (Spinal muscular atrophy) MeSH ID = D014897
- Q158856 (West Nile Virus) MeSH ID = D014901
- Q953638 (Wiskott–Aldrich syndrome) MeSH ID = D014923
- Q1153641 (Wolfram syndrome) MeSH ID = D014929
- Q267602 (XYY syndrome) MeSH ID = D014997
- Q154874 (Yellow fever) MeSH ID = D015004
- Q182672 (Zoonosis) MeSH ID = D015047
- Q583908 (Multi-infarct dementia) MeSH ID = D015161
- Q954831 (Prolactinoma) MeSH ID = D015175
- Q189167 (Zellweger syndrome) MeSH ID = D015211
- Q2622714 (Cholesteryl ester storage disease) MeSH ID = D015217
- Q2061846 (Wolman disease) MeSH ID = D015223
- Q1467339 (hypertriglyceridemia) MeSH ID = D015228
- Q5506342 (Fructose bisphosphatase deficiency) MeSH ID = D015319
- Q7263794 (Pyruvate carboxylase deficiency) MeSH ID = D015324
- Q7263801 (Pyruvate dehydrogenase deficiency) MeSH ID = D015325
- Q845618 (Dejerine–Sottas disease) MeSH ID = D015417
- Q1052687 (Charcot–Marie–Tooth disease) MeSH ID = D015417
- Q2299379 (Membranoproliferative glomerulonephritis) MeSH ID = D015432
- Q264118 (acute myeloid leukemia) MeSH ID = D015470
- Q612108 (Acute promyelocytic leukemia) MeSH ID = D015473
- Q7098792 (Optic disc drusen) MeSH ID = D015594
- Q1066011 (Cowpox) MeSH ID = D015605
- Q1756898 (Lambert–Eaton myasthenic syndrome) MeSH ID = D015624
- Q548719 (Aniridia) MeSH ID = D015783
- Q2397009 (Choroideremia) MeSH ID = D015794
- Q3961677 (Langer–Giedion syndrome) MeSH ID = D015826
- Q521953 (Anisocoria) MeSH ID = D015875
- Q624590 (Arachnoid cyst) MeSH ID = D016080
- Q383228 (Gerstmann–Sträussler–Scheinker syndrome) MeSH ID = D016098
- Q3589131 (Epidermolysis bullosa dystrophica) MeSH ID = D016108
- Q3726862 (Junctional epidermolysis bullosa) MeSH ID = D016109
- Q3124960 (Epidermolysis bullosa simplex) MeSH ID = D016110
- Q2291208 (Sjögren–Larsson syndrome) MeSH ID = D016111
- Q3765145 (Ichthyosis vulgaris) MeSH ID = D016112
- Q3731836 (Congenital ichthyosiform erythroderma) MeSH ID = D016113
- Q3804555 (X-linked ichthyosis) MeSH ID = D016114
- Q1516083 (Piebaldism) MeSH ID = D016116
- Q7077135 (Ocular albinism type 1) MeSH ID = D016117
- Q1459821 (holoprosencephaly) MeSH ID = D016142
- Q220188 (Post-polio syndrome) MeSH ID = D016262
- Q1514476 (Febrile neutrophilic dermatosis) MeSH ID = D016463
- Q2881413 (primary lateral sclerosis) MeSH ID = D016472
- Q863861 (Hailey–Hailey disease) MeSH ID = D016506
- Q4860308 (Bare lymphocyte syndrome) MeSH ID = D016511
- Q1935832 (neurofibromatosis type II) MeSH ID = D016518
- Q1529983 (Hunter syndrome) MeSH ID = D016532
- Q5513690 (GM1 gangliosidoses) MeSH ID = D016537
- Q1750471 (Sly syndrome) MeSH ID = D016538
- Q631904 (Atypical teratoid rhabdoid tumor) MeSH ID = D016543
- Q638729 (Idiopathic thrombocytopenic purpura) MeSH ID = D016553
- Q883850 (Blepharophimosis) MeSH ID = D016569
- Q741713 (Panic disorder) MeSH ID = D016584
- Q804521 (Bacterial vaginosis) MeSH ID = D016585
- Q647630 (Premature ovarian failure) MeSH ID = D016649
- Q5786759 (Lupus anticoagulant) MeSH ID = D016682
- Q1648128 (Ramsay Hunt syndrome type II) MeSH ID = D016697
- Q281115 (Proteus syndrome) MeSH ID = D016715
- Q200781 (Pleural empyema) MeSH ID = D016724
- Q582207 (Antiphospholipid syndrome) MeSH ID = D016736
- Q1544408 (Alagille syndrome) MeSH ID = D016738
- Q326643 (Hepatitis E) MeSH ID = D016751
- Q1044327 (Caroli disease) MeSH ID = D016767
- Q187542 (Li–Fraumeni syndrome) MeSH ID = D016864
- Q877827 (Diabetic ketoacidosis) MeSH ID = D016883
- Q675311 (autoimmune polyendocrine syndrome) MeSH ID = D016884
- Q944777 (Endometrial cancer) MeSH ID = D016889
- Q2732398 (Autosomal dominant polycystic kidney) MeSH ID = D016891
- Q3395618 (Autosomal recessive polycystic kidney) MeSH ID = D017044
- Q1472818 (Common variable immunodeficiency) MeSH ID = D017074
- Q288714 (Alpha-thalassemia) MeSH ID = D017085
- Q3616632 (Beta-thalassemia) MeSH ID = D017086
- Q1759389 (Gunther disease) MeSH ID = D017092
- Q942926 (Selective immunoglobulin A deficiency) MeSH ID = D017098
- Q424247 (Acute intermittent porphyria) MeSH ID = D017118
- Q1479497 (Porphyria cutanea tarda) MeSH ID = D017119
- Q390791 (Hepatoerythropoietic porphyria) MeSH ID = D017121
- Q535364 (Angelman syndrome) MeSH ID = D017204
- Q2666433 (MELAS syndrome) MeSH ID = D017241
- Q1881388 (MERRF syndrome) MeSH ID = D017243
- Q2026857 (Chronic progressive external ophthalmoplegia) MeSH ID = D017246
- Q847605 (neurofibromatosis) MeSH ID = D017253
- Q1754874 (Polysomnography) MeSH ID = D017286
- Q1165179 (Kallmann syndrome) MeSH ID = D017436
- Q3801491 (Epidermolytic hyperkeratosis) MeSH ID = D017488
- Q266421 (Harlequin-type ichthyosis) MeSH ID = D017490
- Q3804556 (Lamellar ichthyosis) MeSH ID = D017490
- Q2166371 (Seborrheic keratosis) MeSH ID = D017492
- Q2256736 (Abdominal aortic aneurysm) MeSH ID = D017544
- Q190370 (Central pontine myelinolysis) MeSH ID = D017590
- Q613809 (Kleine–Levin syndrome) MeSH ID = D017593
- Q1892153 (WAGR syndrome) MeSH ID = D017624
- Q763356 (CREST syndrome) MeSH ID = D017675
- Q2551272 (Hypereosinophilic syndrome) MeSH ID = D017681
- Q371520 (polydactyly) MeSH ID = D017689
- Q4761773 (Aneurysmal bone cyst) MeSH ID = D017824
- Q2349546 (Canavan disease) MeSH ID = D017825
- Q3026441 (Machado–Joseph disease) MeSH ID = D017827
- Q2583514 (Argentine hemorrhagic fever) MeSH ID = D018051
- Q459896 (Cystic hygroma) MeSH ID = D018191
- Q1878759 (Lymphangioleiomyomatosis) MeSH ID = D018192
- Q6949365 (Myxoid liposarcoma) MeSH ID = D018208
- Q1200239 (Dermatofibrosarcoma protuberans) MeSH ID = D018223
- Q4063436 (Alveolar soft part sarcoma) MeSH ID = D018234
- Q1786953 (Seminoma) MeSH ID = D018239
- Q2376518 (Syringoma) MeSH ID = D018252
- Q918285 (Adrenocortical carcinoma) MeSH ID = D018268
- Q256806 (Esthesioneuroblastoma) MeSH ID = D018304
- Q6743515 (Malignant rhabdoid tumour) MeSH ID = D018335
- Q1052913 (Human respiratory syncytial virus) MeSH ID = D018357
- Q1154422 (Leukocyte adhesion deficiency) MeSH ID = D018370
- Q1515038 (Thyroid hormone resistance) MeSH ID = D018382
- Q591256 (MALT lymphoma) MeSH ID = D018442
- Q3043153 (Protein S deficiency) MeSH ID = D018455
- Q125223 (Oxygen toxicity) MeSH ID = D018496
- Q2892779 (Nephrogenic diabetes insipidus) MeSH ID = D018500
- Q3347154 (Multiple endocrine neoplasia type 1) MeSH ID = D018761
- Q2296876 (Tricuspid atresia) MeSH ID = D018785
- Q183134 (Sepsis) MeSH ID = D018805
- Q604075 (Multiple endocrine neoplasia type 2) MeSH ID = D018813
- Q624748 (Multiple endocrine neoplasia type 2b) MeSH ID = D018814
- Q1671412 (Interstitial cystitis) MeSH ID = D018856
- Q684840 (Sneddon's syndrome) MeSH ID = D018860
- Q1636310 (Landau–Kleffner syndrome) MeSH ID = D018887
- Q18767 (Primary progressive aphasia) MeSH ID = D018888
- Q7320761 (Rhizomelic chondrodysplasia punctata) MeSH ID = D018902
- Q362719 (Anterior ischemic optic neuropathy) MeSH ID = D018917
- Q7234207 (Posterior ischemic optic neuropathy) MeSH ID = D018917
- Q970826 (Gulf War syndrome) MeSH ID = D018923
- Q1848471 (Inclusion body myositis) MeSH ID = D018979
- Q558077 (Williams syndrome) MeSH ID = D018980
- Q998273 (Smith–Lemli–Opitz syndrome) MeSH ID = D019082
- Q1145674 (Necrotizing fasciitis) MeSH ID = D019115
- Q51993 (Ebola) MeSH ID = D019142
- Q8064876 (Zaire ebolavirus) MeSH ID = D019142
- Q6029060 (Infantile neuroaxonal dystrophy) MeSH ID = D019150
- Q2280106 (Branchio-oto-renal syndrome) MeSH ID = D019280
- Q2602467 (Cerebrotendineous xanthomatosis) MeSH ID = D019294
- Q488214 (Rolandic epilepsy) MeSH ID = D019305
- Q1409611 (Port-wine stain) MeSH ID = D019339
- Q2555727 (Arrhythmogenic right ventricular dysplasia) MeSH ID = D019571
- Q1541975 (Multiple system atrophy) MeSH ID = D019578
- Q1570013 (Thrombophilia) MeSH ID = D019851
- Q1345792 (Goodpasture's syndrome) MeSH ID = D019867
- Q3709312 (Dyskeratosis congenita) MeSH ID = D019871
- Q1327712 (Alpha 1-antitrypsin deficiency) MeSH ID = D019896
- Q596474 (Conduct disorder) MeSH ID = D019955
- Q2845978 (Stereotypic movement disorder) MeSH ID = D019956
- Q1328833 (Oppositional defiant disorder) MeSH ID = D019958
- Q296104 (Activated protein C resistance) MeSH ID = D020016
- Q5384031 (Epstein–Barr virus infection) MeSH ID = D020031
- Q1495674 (Gastroschisis) MeSH ID = D020139
- Q5513691 (GM2 gangliosidoses) MeSH ID = D020143
- Q1504570 (Protein C deficiency) MeSH ID = D020151
- Q3704732 (Antithrombin III deficiency) MeSH ID = D020152
- Q890367 (Argininemia) MeSH ID = D020162
- Q3043161 (Ornithine transcarbamylase deficiency) MeSH ID = D020163
- Q5037834 (Carbamoyl phosphate synthetase I deficiency) MeSH ID = D020165
- Q1122668 (Tyrosinemia) MeSH ID = D020176
- Q1125121 (Advanced sleep phase disorder) MeSH ID = D020178
- Q979129 (Ondine's curse) MeSH ID = D020182
- Q543517 (Juvenile myoclonic epilepsy) MeSH ID = D020190
- Q2280285 (Dentatorubral-pallidoluysian atrophy) MeSH ID = D020191
- Q163905 (Lafora disease) MeSH ID = D020192
- Q2356131 (Unverricht–Lundborg disease) MeSH ID = D020194
- Q7922751 (Vertebral artery dissection) MeSH ID = D020217
- Q205214 (Guillain–Barré syndrome) MeSH ID = D020275
- Q1088030 (Chronic inflammatory demyelinating polyneuropathy) MeSH ID = D020277
- Q693519 (Essential tremor) MeSH ID = D020329
- Q1418152 (Möbius syndrome) MeSH ID = D020331
- Q1876206 (Pelizaeus–Merzbacher disease) MeSH ID = D020371
- Q520797 (Neuromyotonia) MeSH ID = D020386
- Q1648484 (Duchenne muscular dystrophy) MeSH ID = D020388
- Q1335642 (Emery–Dreifuss muscular dystrophy) MeSH ID = D020389
- Q1399182 (Facioscapulohumeral muscular dystrophy) MeSH ID = D020391
- Q638975 (Central core disease) MeSH ID = D020512
- Q3269843 (Hyperkalemic periodic paralysis) MeSH ID = D020513
- Q622828 (Hypokalemic periodic paralysis) MeSH ID = D020514
- Q2702863 (Thyrotoxic periodic paralysis) MeSH ID = D020514
- Q12202 (stroke) MeSH ID = D020521
- Q7514772 (Silent stroke) MeSH ID = D020521
- Q3273331 (Acatalasia) MeSH ID = D020642
- Q899726 (Spinocerebellar ataxia) MeSH ID = D020754
- Q18576 (Pick's disease) MeSH ID = D020774
- Q1678281 (Bardet–Biedl syndrome) MeSH ID = D020788
- Q782958 (Centronuclear myopathy) MeSH ID = D020914
- Q2563352 (Wernicke–Korsakoff syndrome) MeSH ID = D020915
- Q559435 (Dyssomnia) MeSH ID = D020920
- Q4887956 (Benign familial neonatal epilepsy) MeSH ID = D020936
- Q1331905 (Dementia with Lewy bodies) MeSH ID = D020961
- Q493103 (Paramyotonia congenita) MeSH ID = D020967
- Q192579 (jet lag) MeSH ID = D021081
- Q1506216 (Hermansky–Pudlak syndrome) MeSH ID = D022861
- Q8042656 (XX gonadal dysgenesis) MeSH ID = D023961
- Q657193 (Metabolic syndrome) MeSH ID = D024821
- Q134003 (Haemophilia) MeSH ID = D025861
- Q2756703 (Septo-optic dysplasia) MeSH ID = D025962
- Q935710 (Mitochondrial disease) MeSH ID = D028361
- Q776026 (Biotinidase deficiency) MeSH ID = D028921
- Q5883885 (Holocarboxylase synthetase deficiency) MeSH ID = D028922
- Q2869820 (Kjer's optic neuropathy) MeSH ID = D029241
- Q1262161 (Leber's hereditary optic neuropathy) MeSH ID = D029242
- Q3843807 (Salla disease) MeSH ID = D029461
- Q5160440 (Congenital hypoplastic anemia) MeSH ID = D029502
- Q1208654 (Diamond–Blackfan anemia) MeSH ID = D029503
- Q3304152 (Jervell and Lange-Nielsen syndrome) MeSH ID = D029593
- Q724714 (Romano–Ward syndrome) MeSH ID = D029597
- Q200779 (genetic disorder) MeSH ID = D030342
- Q632228 (Hajdu–Cheney syndrome) MeSH ID = D031845
- Q862872 (Fatal familial insomnia) MeSH ID = D034062
- Q737943 (Streptococcus milleri group) MeSH ID = D034364
- Q12133 (Deafness) MeSH ID = D034381
- Q2581333 (Post-concussion syndrome) MeSH ID = D038223
- Q567820 (Alexander disease) MeSH ID = D038261
- Q1106881 (Coffin–Lowry syndrome) MeSH ID = D038921
- Q3042171 (Oculopharyngeal muscular dystrophy) MeSH ID = D039141
- Q424221 (Acute stress reaction) MeSH ID = D040701
- Q272714 (Gallstone) MeSH ID = D042882
- Q2065747 (Apparent mineralocorticoid excess syndrome) MeSH ID = D043204
- Q1422034 (Cronkhite–Canada syndrome) MeSH ID = D044483
- Q291617 (Beta-mannosidosis) MeSH ID = D044905
- Q669822 (Laron syndrome) MeSH ID = D046150
- Q1495661 (Gastrointestinal stromal tumor) MeSH ID = D046152
- Q823140 (Hereditary coproporphyria) MeSH ID = D046349
- Q275385 (Variegate porphyria) MeSH ID = D046350
- Q1022718 (CADASIL syndrome) MeSH ID = D046589
- Q1535394 (Nesidioblastosis) MeSH ID = D046768
- Q1531322 (Limb-girdle muscular dystrophy) MeSH ID = D049288
- Q5513688 (GM2-gangliosidosis, AB variant) MeSH ID = D049290
- Q5282843 (Distal muscular dystrophy) MeSH ID = D049310
- Q1250362 (Nijmegen breakage syndrome) MeSH ID = D049932
- Q5432934 (Familial dysalbuminemic hyperthyroxinemia) MeSH ID = D050010
- Q773118 (Andersen–Tawil syndrome) MeSH ID = D050030
- Q11094 (Hashimoto's thyroiditis) MeSH ID = D050031
- Q7799746 (Thyroid dysgenesis) MeSH ID = D050033
- Q7847568 (True hermaphroditism) MeSH ID = D050090
- Q1996053 (Chronic pancreatitis) MeSH ID = D050500
- Q1642170 (Hemophagocytic lymphohistiocytosis) MeSH ID = D051359
- Q180913 (Bulimia nervosa) MeSH ID = D052018
- Q5220984 (Danon disease) MeSH ID = D052120
- Q5493754 (Frasier syndrome) MeSH ID = D052159
- Q917399 (Usher syndrome) MeSH ID = D052245
- Q5959167 (Hypoalphalipoproteinemia) MeSH ID = D052456
- Q4780235 (Apolipoprotein B deficiency) MeSH ID = D052476
- Q5160432 (Congenital generalized lipodystrophy) MeSH ID = D052497
- Q3843799 (Multiple sulfatase deficiency) MeSH ID = D052517
- Q2067267 (Niemann–Pick disease, type C) MeSH ID = D052556
- Q1424137 (Subacute combined degeneration of spinal cord) MeSH ID = D052879
- Q6029027 (Infantile Refsum disease) MeSH ID = D052919
- Q8041557 (X-linked hypophosphatemia) MeSH ID = D053098
- Q101452 (2009 flu pandemic) MeSH ID = D053118
- Q737510 (Pulmonary aspiration) MeSH ID = D053120
- Q5957519 (Hyper-IgM syndrome type 3) MeSH ID = D053306
- Q5957524 (Hyper-IgM syndrome type 4) MeSH ID = D053306
- Q4162392 (Meesmann corneal dystrophy) MeSH ID = D053559
- Q5986438 (Ichthyosis bullosa of Siemens) MeSH ID = D053560
- Q1053120 (Gitelman syndrome) MeSH ID = D053579
- Q1423538 (X-linked severe combined immunodeficiency) MeSH ID = D053632
- Q599683 (Brugada syndrome) MeSH ID = D053840
- Q5276448 (Dihydropyrimidine dehydrogenase deficiency) MeSH ID = D054067
- Q5572454 (Glutaric acidemia type 2) MeSH ID = D054069
- Q3043158 (Mevalonate kinase deficiency) MeSH ID = D054078
- Q1544416 (lissencephaly) MeSH ID = D054082
- Q2096745 (Hereditary angioedema) MeSH ID = D054179
- Q1457267 (Schizencephaly) MeSH ID = D054220
- Q2200977 (Miller–Dieker syndrome) MeSH ID = D054221
- Q167050 (Sertoli cell-only syndrome) MeSH ID = D054331
- Q2578247 (Juvenile myelomonocytic leukemia) MeSH ID = D054429
- Q746781 (Neuroacanthocytosis) MeSH ID = D054546
- Q911136 (Degos disease) MeSH ID = D054853
- Q585011 (Antley–Bixler syndrome) MeSH ID = D054882
- Q7104932 (Orthostatic intolerance) MeSH ID = D054971
- Q3085434 (Pallister–Hall syndrome) MeSH ID = D054975
- Q5113988 (Chronic periodontitis) MeSH ID = D055113
- Q1995327 (Spinal and bulbar muscular atrophy) MeSH ID = D055534
- Q1396345 (Farber disease) MeSH ID = D055577
- Q827497 (Muir–Torre syndrome) MeSH ID = D055653
- Q4675304 (Acrocallosal syndrome) MeSH ID = D055673
- Q1752571 (myelofibrosis) MeSH ID = D055728
- Q2039267 (Aspirin-induced asthma) MeSH ID = D055963
- Q779203 (Neonatal onset multisystem inflammatory disease) MeSH ID = D056587
- Q928424 (Barth syndrome) MeSH ID = D056889
- Q425811 (Hypertensive retinopathy) MeSH ID = D058437
Total: 915