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)
Lewy Body Dementia
Lifr Levels
Linoleic Acid to Total Fatty Acids Percentage (ukb Data Field 23456)
Lipa-related Disorder
Lipase Deficiency
Loneliness (linear Analysis)
Long Qt Syndrome 10
Lung Function in Never Smokers (low Fev1 Vs High Fev1)
Male Puberty Timing (early Vs. Average Onset Voice Breaking)
Martsolf Syndrome 1
Maturity-onset Diabetes of the Young Type 8
Medial Orbital Frontal Cortex Volume
Median Relapse-independent Longitudinal Multiple Sclerosis Severity Scale Score in Relapse-onset Multiple Sclerosis
Megf9 Protein Levels
Microcephaly-capillary Malformation Syndrome
Mitf-related Disorder
Moderate Global Developmental Delay
Mthfsd Protein Levels
Multicentric Carpo-tarsal Osteolysis with or Without Nephropathy
Mutilating Keratoderma
Myo18b-related Disorder
N-acetylphenylalanine Levels
N1-methyl-2-pyridone-5-carboxamide Levels
Neurofibroma
Nicotine Withdrawal
Noonan Syndrome-like Disorder with Loose Anagen Hair 1
Obesity Due to Pro-opiomelanocortin Deficiency
Occlusion and Stenosis of Precerebral Arteries (phecode 433.1)
Oligodontia
Osteogenesis Imperfecta Type 10
Osteogenesis Imperfecta Type 15
Other Hypertrophic Cardiomyopathy (phecode 425.12)
P Wave Duration
Paget Disease of Bone 3
Pain
Palmitoyl Dihydrosphingomyelin (d18:0/16:0) Levels
Pappalysin-1 Levels
Parkinsonism-dystonia
Pdl1 Levels
Peroxisome Biogenesis Disorder 8a (zellweger)
Phosphatidylcholine (15:0_20:4) Levels
Phosphatidylcholine_34:0_[m+h]1+/phosphatidylethanolamine_37:0_[m+h]1+/phosphatidate_39:1_[m+nh4]1+ Levels
Phosphatidylinositol (18:0_18:2) Levels
Phosphatidylinositol(34:1)_[m-h]1- Levels
Phosphatidylinositol(35:2)_[m-h]1- Levels
Phosphatidylinositol(40:5)_[m-h]1- Levels
Pi16 Protein Levels
Pklr-related Disorder
Plasma Factor V Levels (parent of Origin Effect) X Rs75463553 Interaction
Plasma Omega-3 Polyunsaturated Fatty Acid Levels (alphalinolenic Acid)
Polycystic Ovary Syndrome in Overweight/obese Individuals (bmi > 25 Kg/m2)
Pontocerebellar Hypoplasia Type 5
Posterior Cortical Atrophy and Alzheimer's Disease
Ppy Protein Levels
Preeclampsia (maternal Genotype Effect)
Primary Ciliary Dyskinesia 20
Primary Failure of Tooth Eruption
Programmed Cell Death 1 Ligand 2 Levels
Progressive Myoclonic Epilepsy Type 5
Prostate Cancer (advanced)
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