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)
Scarlet Fever
Senior-loken Syndrome 1
Serum Metabolite Ratios in Chronic Kidney Disease
Skin Reflectance (melanin Index)
Sodium (maximum, Inv-norm Transformed)
Spinal Muscular Atrophy
Subcutaneous Adipose Tissue
Sudden Cardiac Arrest
Systolic Blood Pressure (cigarette Smoking Interaction)
Tgoln2 Protein Levels
X-linked Hydrocephalus Syndrome
5-acetylamino-6-amino-3-methyluracil Levels
Adverse Response to Drug
Age-related Macular Degeneration or Covid-19 Critical Illness (mtag)
Age-related Macular Degeneration or Covid-19 Hospitalization (mtag)
Age-related Macular Degeneration or Covid-19 Infection (mtag)
Allergic Disease (asthma, Hay Fever And/or Eczema) (age of Onset)
Alpi Protein Levels
Alzheimer's Disease, Proxy Alzheimer's Disease or Related Dementias in Apoe E4 Carriers
And Delayed Development Syndrome
Arthritis (juvenile Idiopathic)
Atp7b-related Disorder
Autosomal Recessive Spinocerebellar Ataxia 10
Bche Protein Levels
Branchiootorenal Syndrome 1
Cblif Protein Levels
Cd209 Protein Levels
Cholesterol to Total Lipids in Very Small Vldl Percentage (ukb Data Field 23605)
Cholesteryl Ester Levels in Medium Ldl
Col4a5-related Disorder
Congenital Contractures of the Limbs and Face
Congenital Factor Vii Deficiency
Congenital Muscular Dystrophy
Congenital Muscular Dystrophy Due to Lmna Mutation
Coronary Artery Calcified Atherosclerotic Plaque Score in Type 2 Diabetes
Crouzon Syndrome
Ctrb1 Protein Levels
D-2-hydroxyglutaric Aciduria 1
Diacylglycerol(36:2)_[m+h-h2o]1+ Levels
Diffuse Pediatric-type High-grade Glioma
Dihydropteridine Reductase Deficiency
Eotaxin Levels
Eppk1 Protein Levels
Fruit Consumption
Group G
H3-wildtype and Idh-wildtype
Hdl X Low Social Support Interaction (2df Test)
Hereditary Spastic Paraplegia 5a
Hyperthyroidism
Hypobetalipoproteinemia
Idua Protein Levels
Infantile Myofibromatosis
Infantile-onset
Intake of Total Sugars
Iris Color (l* Coordinate)
Lamb1 Protein Levels
Leprechaunism Syndrome
Mitochondrial Short-chain Enoyl-coa Hydratase 1 Deficiency
Mitochondrial Trifunctional Protein Deficiency 1
Mmp3 Protein Levels
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