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)
Multiple Sclerosis (age of Onset)
Multiple System Atrophy 1
Musculocontractural Type 2
Mxra8 Protein Levels
Mycobacterium Tuberculosis
Myh14-related Disorder
Myosclerosis
N-acetylhistidine Levels
Nedba
Neovascular Age-related Macular Degeneration
Nephrocalcinosis
Neurodevelopmental Disorder with or Without Variable Brain Abnormalities
Neurodevelopmental Disorders
Neuropathic Pain
Neuropathologic Traits (pleiotropy)
Neutral Antibody Levels in Response to Sars-cov-2 Vaccination
Nlrp3-related Disorder
Nuclear Type 19
Obesity Due to Melanocortin 4 Receptor Deficiency
Obstructive Azoospermia
Occipital Thickness (unadjusted For Global Measures)
Oral Glucose Tolerance Test-1h
Osteopetrosis with Renal Tubular Acidosis
Other Anemias (phecode 285)
Overall Survival in Advanced Colorectal Cancer
Parental Longevity (father's Attained Age)
Pecam1 Protein Levels
Pediatric Bone Mineral Density (femoral Neck)
Pelvic Height
Peripheral Vascular Disease, Unspecified (phecode 443.9)
Pettigrew Syndrome
Peyronie's Disease (phecode 604.3)
Phobia (phecode 300.13)
Phosphate Levels
Phosphatidylcholine_34:1_[m+h]1+/phosphatidylethanolamine_37:1_[m+h]1+/phosphatidate_39:2_[m+nh4]1+ Levels
Phosphatidylcholine_44:5_[m+oac]1- Levels
Phosphatidylcholine(45:0)_[m-h]1- Levels
Phosphatidylethanolamine-o_36:4_[m-h]1-/phosphatidylethanolamine-p_36:3_[m-h]1- Levels
Phosphatidylethanolamine-o_38:6_[m-h]1-/phosphatidylethanolamine-p_38:5_[m-h]1- Levels
Phosphatidylserine_40:3_[m+h]1+/phosphatidylglycerol_40:5_[m+nh4]1+ Levels
Phosphorus Levels
Pik3ca-related Disorder
Plasma Omega-3 Polyunsaturated Fatty Acid Levels (docosahexaenoic Acid)
Pnkp-related Disorder
Polydactyly of A Triphalangeal Thumb
Pontocerebellar Hypoplasia Type 2b
Primary Ciliary Dyskinesia 27
Primary Ciliary Dyskinesia 29
Pseudo-torch Syndrome 1
Pseudohypoaldosteronism Type 2d
Qrs Complex (cornell)
Qrs Interval (sulfonylurea Treatment Interaction)
Qt Dynamics During Exercise
Qt Interval (drug Interaction)
Rapidly Progressive Alzheimer's Disease (clinical Vs Typical) (case-control Set 1)
Rapidly Progressive Alzheimer's Disease (clinical Vs Typical) (case-control Set 3)
Rasa1-related Disorder
Rbc Levels of 15-hete
Reactive Lymphocyte Count
Regional Cortical Thickness (precuneus)
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →