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)
Arrhythmogenic Right Ventricular Dysplasia 9
Alport Syndrome
Neurofibromatosis-noonan Syndrome
Saturated Fatty Acids to Total Fatty Acids Percentage
Dystrophin Deficiency
Zellweger Spectrum Disorders
Personality Traits or Cognitive Traits (multivariate Analysis)
Severe Combined Immunodeficiency
Amyotrophic Lateral Sclerosis Type 4
B Cell-negative
Autosomal Recessive Nonsyndromic Hearing Loss 4
Electrocardiogram Morphology (amplitude At Temporal Datapoints)
What Is Your Height? (cm, Inv-normal Transformed)
Autosomal Dominant 1
Non-albumin Protein Levels
T Cell-negative
Autosomal Recessive Limb-girdle Muscular Dystrophy
High Light Scatter Reticulocyte Percentage (ukb Data Field 30290)
Impedance of Whole Body (ukb Data Field 23106)
Dilated Cardiomyopathy 1dd
Landau-kleffner Syndrome
Fetal Akinesia Deformation Sequence 1
Junctional Epidermolysis Bullosa Gravis of Herlitz
Congenital Hyperammonemia
Lymphocyte Count (ukb Data Field 30120)
Norman-roberts Syndrome
Body Fat Percentage
Corneal Resistance Factor (mtag)
Glanzmann Thrombasthenia
Pseudo-hurler Polydystrophy
Gamma Glutamyl Transpeptidase
Hypertrophic Cardiomyopathy 4
Telomere Length (principal Component 1)
Type 7
Cardiovascular Disease
Waist Circumference
Bethlem Myopathy 2
Fluid Intelligence Score (baseline)
Multiple Types
Autosomal Dominant 2
Deficiency of Alpha-mannosidase
Free Testosterone Levels
Mps-iv-a
Concentration of Large Hdl Particles
Haematocrit Percentage (ukb Data Field 30030)
Ullrich Congenital Muscular Dystrophy 2
Cigarettes Smoked Per Day
Pr Interval
Wolfram Syndrome 1
Menkes Kinky-hair Syndrome
Congenital Bilateral Aplasia of Vas Deferens From Cftr Mutation
Galactosylceramide Beta-galactosidase Deficiency
Autosomal Recessive 5
Congenital Multicore Myopathy with External Ophthalmoplegia
Restless Legs Syndrome
Usher Syndrome Type 2c
Depressive Symptoms
Familial Spinal
Hypertrophic Cardiomyopathy 1
Rubinstein-taybi Syndrome Due to Crebbp Mutations
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