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)
Left Atrial Minimum Volume
Left Molecular Layer Hippocampal Volume (head)
Left Ventricular End Diastole Anterospetal Wall Thickness
Left Ventricular End Systole Anterolateral Wall Thickness
Left Ventricular Hypertrophy
Left Ventricular Noncompaction 7
Left Ventricular Obstructive Tract Defect (maternal Effect)
Leucine Levels (ukb Data Field 23466)
Leukemia (phecode 204)
Lignoceroylcarnitine (c24) Levels
Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] Levels
Lipoma (phecode 214)
Lipoprotein-associated Phospholipase A2 Activity
Lissencephaly 10
Lissencephaly 6 with Microcephaly
Logical Memory (immediate Recall) in Normal Cognition
Long Qt Syndrome 15
Longitudinal Change in Brain Amyloid Plaque Burden
Low Affinity Immunoglobulin Gamma Fc Region Receptor Iii-b Levels
Low-density Lipoprotein Receptor-related Protein 11 Levels
Lpin1-related Disorder
Ltbp3-related Disorder
Lung Function
Lymphocyte Telomere Length
Lyn/tacc3 Protein Level Ratio
Lysophosphatidic Acid Phosphatase Type 6 Levels
Lysophosphatidylcholine (20:3) [sn1] Levels
Macrophage Colony-stimulating Factor 1 Receptor Levels
Major Depressive Disorder (probable)
Major Depressive Disorder Vs Adhd (ordinary Least Squares (ols))
Male Infertility (sertoli Cell-only)
Manf Protein Levels
Manlignant and Unknown Neoplasms of Brain and Nervous System (phecode 191)
Mannose-binding Lectin Deficiency
Map2k6/tbl1x Protein Level Ratio
Map4k5/tbcb Protein Level Ratio
Mapt-related Disorder
Max Protein Levels
Mcfd2 Protein Levels
Mean Arterial Pressure (alcohol Consumption Interaction)
Mean Degree of Stenosis
Medication Use (anti-inflammatory and Antirheumatic Products, Non-steroids)
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2b
Melorheostosis
Merrf Syndrome
Metabolic Syndrome (multivariate Analysis)
Metabolically Unhealthy in Normal Weight
Metabolite Levels (hva/5-hiaa Ratio)
Metap1d/vash1 Protein Level Ratio
Mhc Class Ii Deficiency 3
Mhc Class Ii Deficiency 4
Mica-micb Heterodimer Protein Levels
Microcornea-myopic Chorioretinal Atrophy
Microspherophakia
Mid-trimester Cervical Length (latent Growth Curve Intercept)
Midgestational Circulating Levels of Pbdes (fetal Genetic Effect)
Migraine (mtag)
Mitochondrial Complex Iii Deficiency Nuclear Type 4
Mitochondrial Dna Depletion Syndrome 20 (mngie Type)
Mitochondrial Non-syndromic Sensorineural Hearing Loss
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