Entity directory

Browse phenotypes

Move from normalized entities to their supporting publications and exact evidence sentences.

GenesVariantsPhenotypesPopulations
diabetes mellitus2,1562,156 articlesepilepsyHP:00012502,0842,084 articlesCOVID-191,3171,317 articlesbreast cancer1,2111,211 articlesautism spectrum disorderHP:0000729881881 articlesobesityHP:0001513856856 articleshypertension828828 articlessickle cell diseaseHP:0001878828828 articlesintellectual disabilityHP:0001249736736 articlescolorectal cancer708708 articlesinflammatory bowel disease693693 articleshearing lossHP:0000365663663 articlesleukemia652652 articlescardiomyopathyHP:0001638618618 articlesarrhythmia555555 articlesstroke555555 articlesrenal failure523523 articlesulcerative colitis492492 articlesdevelopmental delayHP:0001263480480 articlesAlzheimer disease455455 articlesneurodevelopmental disorderHP:0012759450450 articlesCrohn disease435435 articleslymphoma428428 articleshepatitis C421421 articleshepatocellular carcinoma417417 articlesthalassemiaHP:0001878409409 articlestuberculosis405405 articleslung cancer398398 articlescongenital heart disease363363 articlesSARS347347 articlesdyslipidemia338338 articlessickle cell anemiaHP:0001878336336 articlescoronary artery disease314314 articlesasthma285285 articlesParkinson disease280280 articlesmyocardial infarction274274 articleshepatitis B255255 articlesmultiple sclerosis236236 articlesmalaria232232 articlesMERS230230 articlesprostate cancer218218 articlesthyroid cancer216216 articlesrheumatoid arthritis212212 articlesinfertility199199 articlessystemic lupus erythematosus191191 articlesovarian cancer173173 articlesDown syndrome171171 articlescongenital cataract165165 articlesfamilial hypercholesterolemiaHP:0003124165165 articlescystic fibrosis157157 articlesHIV infection146146 articlesmetabolic syndrome141141 articlescongenital myopathy134134 articlesatopic dermatitis132132 articleshemophilia122122 articlesretinal dystrophyHP:0000556121121 articlesglucose-6-phosphate dehydrogenase deficiency118118 articlesnephrotic syndrome108108 articlesgastric cancer106106 articlesamyotrophic lateral sclerosis105105 articlesinborn error of metabolismHP:00019399999 articlesretinitis pigmentosa8888 articlespre-eclampsia8484 articlescleft lip and palate8080 articlesceliac disease7474 articlesprimary congenital glaucoma7070 articlespolycystic kidney disease6666 articlesmultiple myeloma6363 articleslysosomal storage diseaseHP:00035415050 articlesendometrial cancer4949 articlesskeletal dysplasia4949 articlesspinal muscular atrophy4545 articleslong QT syndrome4444 articlesDuchenne muscular dystrophy4040 articlesmucopolysaccharidosisHP:00081553737 articlesrecurrent pregnancy loss3636 articlesfamilial Mediterranean fever3434 articlesallergic rhinitis3030 articlesarthrogryposis3030 articlesphenylketonuria2929 articlesprimary ciliary dyskinesia2929 articlesosteogenesis imperfecta2727 articlesLeber congenital amaurosis2626 articlesGaucher disease2525 articlesvon Willebrand disease2525 articlesBardet-Biedl syndrome2424 articlesTurner syndrome2323 articlesNiemann-Pick disease2121 articlesmaple syrup urine disease2121 articlesEhlers-Danlos syndrome1919 articlesFabry disease1919 articlesKlinefelter syndrome1919 articlesMarfan syndrome1919 articleshomocystinuria1919 articlesglycogen storage diseaseHP:00035421818 articlesAlstrom syndrome1414 articlesPompe disease1111 articlesAlport syndrome99 articlesNoonan syndrome88 articlesBecker muscular dystrophy44 articles