Health Conditions
43,676 conditions with known genetic associations in our database.
All(43,676)
Other(43,676)
Cardiovascular(1,793)
Metabolic(1,614)
Renal(1,319)
Cancer(1,257)
Neurological(750)
Ophthalmic(535)
Gastrointestinal(367)
Hematologic(345)
Respiratory(323)
Autoimmune(265)
Dermatologic(221)
Pharmacogenomic(163)
Musculoskeletal(129)
Phosphatidylethanolamine_34:2_[m-h]1- Levels
Phosphatidylglycerol(34:0)_[m-h]1- Levels
Pltp Protein Levels
Ritscher-schinzel Syndrome
Schuurs-hoeijmakers Syndrome
Scn1a-related Disorder
Sele Protein Levels
Seropositivity For Streptococcus Agalactiae Peptide (agilent_241118)
Seropositivity For Streptococcus Pyogenes Peptide (agilent_241884)
Smpd1-related Disorder
Strep Throat
Subjective Well-being (mtag)
Tnr Protein Levels
Top1 Protein Levels
Total Omega-3 Fatty Acid Levels
Triacylglycerol(54:3)_[m+nh4]1+ Levels
Triglycerides to Phosphoglycerides Ratio (ukb Data Field 23435)
Type B14
Vaginal Microbiome Metacyc Pathway (pwy-5180|toluene Degradation I (aerobic) (via O-cresol))
Vaginal Microbiome Metacyc Pathway (pwy-5741|ethylmalonyl-coa Pathway)
Vwf Levels
With Wooly Hair
X-linked Intellectual Disability-psychosis-macroorchidism Syndrome
Acetoacetate Levels
Afap1 Protein Levels
Ahsg Protein Levels
And Dysequilibrium Syndrome 1
Apolipoprotein A1 Levels (ukb Data Field 23440)
Au-kline Syndrome
Autosomal Dominant Limb-girdle Muscular Dystrophy Type 1f
Autosomal Recessive 42
Autosomal Recessive Bestrophinopathy
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2m
Autosomal Recessive Nonsyndromic Hearing Loss 28
Bardet-biedl Syndrome 15
Barrett's Esophagus
Blmh Protein Levels
Ccn4 Protein Levels
Cerebrospinal Fluid Ab1-42 Levels
Cerebrospinal Fluid T-tau:ab1-42 Ratio
Charcot-marie-tooth Disease Axonal Type 2f
Cndp1 Protein Levels
Cold Induced Vasodilation
Concentration of Large Vldl Particles (ukb Data Field 23495)
Congenital Myasthenic Syndrome 12
Corpus Callosum Total Area
Creld1 Protein Levels
Crigler-najjar Syndrome
Cstb Protein Levels
Ctcf-related Neurodevelopmental Disorder
Deficiency of Hyaluronoglucosaminidase
Desanto-shinawi Syndrome Due to Wac Point Mutation
Dilated Cardiomyopathy 1r
Dorsolateral Prefrontal Area (unadjusted For Global Measures)
Dpagt1-congenital Disorder of Glycosylation
Dxa-bone Mineral Density (pelvis) (ukb Data Field 23232)
Fg Syndrome 1
Flcn-related Disorder
Flnc-related Disorder
Frailty (general Factor)
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