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)
Sum Eosinophil Basophil Counts
Tonsillectomy
Type B1
White Matter Microstructure (mean Diusivities)
Amyotrophic Lateral Sclerosis
Charcot-marie-tooth Disease Dominant Intermediate E
Cholesterol Levels in Chylomicrons and Extremely Large Vldl
Diastrophic Dysplasia
Free Cholesterol in Medium Hdl
Sleep Duration
Total Concentration of Lipoprotein Particles
Type A2
White Blood Cell Count (wbc, Maximum, Inv-norm Transformed)
11p Partial Monosomy Syndrome
Childhood-onset
Medication Use (calcium Channel Blockers)
Medication Use (drugs Used in Diabetes)
Thyrotoxic Periodic Paralysis
Triglycerides to Total Lipids in Large Hdl Percentage
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2d
Dilated Cardiomyopathy 3b
Frontotemporal Dementia
Heimler Syndrome 1
Retinitis Pigmentosa 19
Edge-level Brain Connectivity (multivariate Analysis)
Hereditary Hemochromatosis
Histiocytic Medullary Reticulosis
Neonatal
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 5
Autosomal Recessive Nonsyndromic Hearing Loss 23
Body Fat Percentage (ukb Data Field 23099)
Concentration of Small Hdl Particles
Gut Microbiome Abundance (class Clostridium Sensu Stricto Sp. 17 (at 1 Year) X Exclusive Breastfeeding (6 Months) Interaction
Night Sleep Phenotypes
Nonsyndromic Genetic Hearing Loss
Type 5
Vitamin D Levels
Bardet-biedl Syndrome 2
Blood Cell Traits Latent Factor 25 (white Cell)
Coronary Artery Disease (mtag)
Hereditary Spastic Paraplegia 7
Nephrolithiasis/nephrocalcinosis
Of Infancy
Serum Phosphate Levels
Tyrosinase-positive Oculocutaneous Albinism
Tyrosinemia Type I
Abdominal Aortic Aneurysm
Arterial Calcification
Body Mass Index (bmi, Minimum, Inv-normal Transformed)
Cerebral Arteriopathy
Dyrk1a-related Intellectual Disability Syndrome
Familial Dysautonomia
Localized or Generalized Intermediate
Papillary Renal Cell Carcinoma Type 1
Retinitis Pigmentosa 20
Total Amyloid (snp X Snp Interaction)
Triglycerides in Very Large Vldl
With Subcortical Infarcts and Leukoencephalopathy
Brain Small Vessel Disease 1 with or Without Ocular Anomalies
Coronary Heart Disease
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