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)
R-6-hydroxywarfarin Levels
Rheumatoid Arthritis (acpa-positive)
Atrial Fibrillation/atrial Flutter
Atypical Hemolytic-uremic Syndrome with C3 Anomaly
Baraitser-winter Syndrome 1
Basophil (absolute Count, Mean, Inv-norm Transformed)
Cholesterol Levels in Large Vldl
Cholesterol to Total Lipids Ratio in Small Vldl
Cholesteryl Ester Levels in Very Large Vldl
Cholesteryl Esters in Idl
Cholesteryl Esters to Total Lipids in Medium Ldl Percentage
Cholesteryl Esters to Total Lipids Ratio in Large Ldl
Cognitive Ability (mtag)
Col1a1-related Disorder
Cone-rod Dystrophy 12
Corneal Dystrophy-perceptive Deafness Syndrome
Coronary Artery Disease or Factor Viii Levels (pleiotropy)
Crohn's Disease (tractor Method with European Ancestry)
Deficiency of Guanidinoacetate Methyltransferase
Familial Temporal Lobe
Fcn2 Protein Levels
Free Cholesterol Levels in Very Large Vldl
Holoprosencephaly 9
Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome
Hypertension (phecode 401)
Il17rb Protein Levels
Macrocephaly
Mps-i-h/s
Neurodevelopmental Disorder with Coarse Facies and Mild Distal Skeletal Abnormalities
Neuropathic Ocular Pain
Neuroticism Conditioned On Highest Math Class (multi-trait Conditioning and Joint Analysis)
Paget Disease of Bone 2
Periventricular White Matter Hyperintensities
Phosphatidylcholine(33:2)_[m+h]1+/phosphatidylethanolamine(36:2)_[m+h]1+/phosphatidate(38:3)_[m+nh4]1+ Levels
Prostate-specific Antigen (psa, Minimum, Inv-norm Transformed)
Smoking Cessation (mtag)
Triglycerides to Total Lipids in Large Vldl Percentage
Triglycerides to Total Lipids Ratio in Large Vldl
Ulcerative Colitis (tractor Method with European Ancestry)
Aggressive 1
And Seizures
Auditory Neuropathy
Autosomal Dominant Childhood-onset Proximal Spinal Muscular Atrophy with Contractures
Autosomal Recessive Nonsyndromic Hearing Loss 8
Basal Cell Nevus Syndrome 1
Brown Vs. Black Hair Color
Brugada Syndrome 8
Calcium (mean, Inv-norm Transformed)
Cholesterol in Idl
Coronary Artery Disease or Factor Xi Levels (pleiotropy)
Coronary Atherosclerosis (phecode 411.4)
Free Cholesterol Levels in Large Ldl
Hypothyroidism (phecode 244)
Ift172-related Disorder
Loeys-dietz Syndrome 4
Lpa Protein Levels
Mean Corpuscular Haemoglobin Concentration (ukb Data Field 30060)
Mitochondrial Dna Depletion Syndrome 4b
Myasthenic Syndrome
Nance-horan Syndrome
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