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)
Coffee Consumption
Forced Vital Capacity Fvc Z Score (ukb Data Field 20257)
King Denborough Syndrome
Proximal
Triglycerides in Large Hdl
Ascending Aorta Diameter
Aspartate Aminotransferase (ast, Mean, Inv-norm Transformed)
Autosomal Dominant Nonsyndromic Hearing Loss 65
Congenital Factor V Deficiency
Encephalopathy Due to Glut1 Deficiency
Hermansky-pudlak Syndrome 1
Myoclonic Dystonia 11
Myopathic Form
Node-level Brain Connectivity (multivariate Analysis)
Pseudohypoaldosteronism Type 2c
Sjögren-larsson Syndrome
Asphyxiating Thoracic Dystrophy 5
Familial Infantile Myasthenia
Hypertrophic Cardiomyopathy 2
Icam2 Protein Levels
Kabuki Syndrome 2
Mitochondrial Dna Depletion Syndrome 1
Peroxisome Biogenesis Disorder 4a (zellweger)
Pyruvate Dehydrogenase E3 Deficiency
Rpe65-related Recessive Retinopathy
Senior-loken Syndrome 8
Spondyloepimetaphyseal Dysplasia
Carnitine Palmitoyl Transferase Ii Deficiency
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
Neutropenia
Rbc Levels of Pyruvate (um)
Upshaw-schulman Syndrome
And Behavioral Abnormalities
Arginase Deficiency
Combined
Complement Factor H-related Protein 3 Levels
Familial Hemophagocytic Lymphohistiocytosis 5
Mckusick Type
Microphthalmia
Pigmented Paravenous Retinochoroidal Atrophy
Spermatogenic Failure 18
Total Corpus Callosum Volume
Hyperimmunoglobulin D with Periodic Fever
Hypertrophic Cardiomyopathy 14
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →