Health Conditions
43,676 conditions with known genetic associations in our database.
All(43,676)
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)
Lrrn1 Protein Levels
Lymphatic Malformation 6
Morquio Syndrome
Neurodegeneration with Brain Iron Accumulation
Optic Atrophy 3
Phosphatidylcholine(38:5)_[m+h]1+/phosphatidylethanolamine(41:5)_[m+h]1+/phosphatidate(43:6)_[m+nh4]1+ Levels
Pinlyp Protein Levels
Pvr Protein Levels
Sema3g Protein Levels
Slamf7 Protein Levels
Tcn2 Protein Levels
Tp53-related Disorder
Type A9
With Psychomotor Retardation and Characteristic Facies 2
Alg12-congenital Disorder of Glycosylation
Alkaline Phosphatase Levels
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2f
Bernard Soulier Syndrome
Body Fat Distribution (arm Fat Ratio)
Caudate Iron Levels (quantitative Susceptibility Mapping)
Diabetic Retinopathy (phecode 250.7)
Diacylglycerol(34:2)_[m+h-h2o]1+ Levels
Dilated Cardiomyopathy 1cc
Electrocardiographic Traits (multivariate)
Emery-dreifuss Muscular Dystrophy
Fatty Acid(22:4)_[m-h]1- Levels
Feeling Miserable
Fluid Intelligence
Hair Colour (natural, Before Greying): Dark Brown (ukb Data Field 1747_4)
Hsbp1 Protein Levels
Lilrb1 Protein Levels
Marshall-smith Syndrome
Meniere Disease
Mitochondrial Hypertrophic Cardiomyopathy with Lactic Acidosis Due to Mto1 Deficiency
Muc2 Protein Levels
Neurofibrillary Tangles
Peak Expiratory Flow (ukb Data Field 3064)
Retinitis Pigmentosa 40
Sphingomyelin_38:1_[m+h]1+ Levels
Thrombocytopenia 2
Total Omega-6 Fatty Acid Levels
Vcan Protein Levels
Autosomal Dominant Nonsyndromic Hearing Loss 3a
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2p
Basal Ganglia Structure
Bell's Palsy
Breast Area
Cd177 Protein Levels
Cerebrospinal Fluid Biomarker Levels
Cholesteryl Ester Levels in Small Ldl
Coffee Consumption (cups Per Day)
Congenital Myasthenic Syndrome 4b
Cranioectodermal Dysplasia 4
Cxcl10 Levels
Dysmorphic Facial Features
East Syndrome
Fibromuscular Dysplasia
Fras1-related Disorder
Fructose-biphosphatase Deficiency
Genetic Non-acquired Premature Ovarian Failure
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