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