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)
Apparent Mineralocorticoid Excess
Arthrogryposis Multiplex Congenita 1
Atr-related Disorder
Atrioventricular Septal Defect
Autosomal Dominant 58
Autosomal Dominant Isolated Somatotropin Deficiency
Autosomal Dominant Mitochondrial Myopathy with Exercise Intolerance
Autosomal Recessive 47
Autosomal Recessive Nonsyndromic Hearing Loss 70
Autosomal Recessive Nonsyndromic Hearing Loss 84a
Ayme-gripp Syndrome
B Subunit
Biliary Tract Abnormality
Bilirubin (z,z) Levels
Blood Group--lutheran Inhibitor
Bmper Protein Levels
Body Fat Percentage and Triglycerides (pairwise)
Body Mass Index X Sex X Age Interaction (4df Test)
Branched-chain, Straight-chain, or Cyclopropyl 10:1 Fatty Acid (1) Levels
Bread Consumption (slices Per Week) (ukb Data Field 1438)
Brugada Syndrome 6
C-c Motif Chemokine 4-like Levels
C-c Motif Chemokine 7 Levels
Carboxypeptidase B2 Levels
Cataract 17 Multiple Types
Ccl22 Protein Levels
Ccl23 Levels
Ccl26 Protein Levels
Cdhr1-related Disorder
Cdk5rap2-related Disorder
Cdkn2d/tbl1x Protein Level Ratio
Cednik Syndrome
Cerebrospinal Fluid Immune Biomarker Levels
Charcot-marie-tooth Disease Dominant Intermediate F
Childhood Wheezing (mid-childhood Remitting)
Cholestasis-pigmentary Retinopathy-cleft Palate Syndrome
Choline Levels (advanced Age)
Choline Levels (elderly Offspring)
Chromosome 2p16.3 Deletion Syndrome
Circulating Odd-numbered Chain Saturated Fatty Acid Levels (c15:0)
Circulating Odd-numbered Chain Saturated Fatty Acid Levels (c15:0+c17:0)
Circulating Odd-numbered Chain Saturated Fatty Acid Levels (c17:0)
Circulating Odd-numbered Chain Saturated Fatty Acid Levels (c19:0)
Circulating Odd-numbered Chain Saturated Fatty Acid Levels (c23:0)
Citrulline Levels
Clec12a Protein Levels
Clec1b Protein Levels
Clmp Protein Levels
Cmin At Steady-state of Apixaban
Cmrf35-like Molecule 6 Levels
Coffin-siris Syndrome 10
Combined Oxidative Phosphorylation Defect Type 21
Combined Oxidative Phosphorylation Deficiency 35
Complement Component 9 Deficiency
Complement Factor H-like 1 Protein Levels
Conduct Disorder (maternal Expressed Emotions Interaction)
Conduct Disorder (symptom Count)
Congenital Myopathy 23
Copine-1 Levels
Cortical Amyloid Beta Load
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →