Health Conditions
52,757 conditions with known genetic associations in our database.
All(52,757)
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)
Type 9
Verbal Learning
Visceral
Bipolar Disorder (mtag)
Cholesterol to Total Lipids in Large Ldl Percentage
Coffee Consumption
Forced Vital Capacity Fvc Z Score (ukb Data Field 20257)
King Denborough Syndrome
Proximal
Triglycerides in Large Hdl
Triglycerides to Total Lipids Ratio in Idl
Triglycerides to Total Lipids Ratio in Very Small Vldl
Ascending Aorta Diameter
Aspartate Aminotransferase (ast, Mean, Inv-norm Transformed)
Autosomal Dominant Nonsyndromic Hearing Loss 65
Cholesterol Levels in Large Hdl
Congenital Factor V Deficiency
Encephalopathy Due to Glut1 Deficiency
Hermansky-pudlak Syndrome 1
Myoclonic Dystonia 11
Myopathic Form
Node-level Brain Connectivity (multivariate Analysis)
Progressive Familial Heart Block Type Ib
Pseudohypoaldosteronism Type 2c
Sjögren-larsson Syndrome
Alzheimer Disease 3
Asphyxiating Thoracic Dystrophy 5
Autosomal Dominant Familial Hematuria-retinal Arteriolar Tortuosity-contractures Syndrome
Familial Infantile Myasthenia
Hypertrophic Cardiomyopathy 2
Icam2 Protein Levels
Kabuki Syndrome 2
Metabolic Dysfunction-associated Steatotic Liver Disease (mtag)
Mitochondrial Dna Depletion Syndrome 1
Peroxisome Biogenesis Disorder 4a (zellweger)
Pyruvate Dehydrogenase E3 Deficiency
Rpe65-related Recessive Retinopathy
Senior-loken Syndrome 8
Spondyloepimetaphyseal Dysplasia
Total Cholesterol (maximum, Inv-norm Transformed)
Age-related Macular Degeneration
Carnitine Palmitoyl Transferase Ii Deficiency
Endometriosis or Asthma (pleiotropy)
Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss
Multiple Sulfatase Deficiency
Nonsyndromic Cleft Palate
Polydactyly
Salla Disease
Thrombocytopenia 1
Triglyceride Levels in Ldl
Vanishing White Matter Disease
X-linked Severe Congenital Neutropenia
And Ophthalmoplegia
Cholesteryl Ester Levels in Large Hdl
Complex Ventricular Septal Defect
Covid-19 (hospitalized Vs Tested, Not Hospitalized)
Dilated Cardiomyopathy 1d
Leber Congenital Amaurosis 7
Lethal Acantholytic Epidermolysis Bullosa
Lifetime Smoking Index
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →