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)
Severe Neonatal-onset Encephalopathy with Microcephaly
Short Stature
Aspartate Aminotransferase Levels (ukb Data Field 30650)
Charcot-marie-tooth Disease Axonal Type 2v
Long Chain 3-hydroxyacyl-coa Dehydrogenase Deficiency
Multiple Endocrine Neoplasia Type 2a
Central Corneal Thickness (mtag)
Cholestasis
Severe X-linked Myotubular Myopathy
Autosomal Recessive Distal Spinal Muscular Atrophy 1
Concentration of Very Large Vldl Particles
Autosomal Dominant 4
Autosomal Recessive Nonsyndromic Hearing Loss 77
Concentration of Large Vldl Particles
Ornithine Carbamoyltransferase Deficiency
Well-being Spectrum (multivariate Analysis)
Autosomal Dominant Nonsyndromic Hearing Loss 6
Gne Myopathy
Leber Congenital Amaurosis 2
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions
Red Cell Diameter Width (rdw, Mean, Inv-norm Transformed)
Tooth Agenesis
Total Protein Levels (ukb Data Field 30860)
Blood Cell Traits Latent Factor 9 (white Cell)
Cbs-related
Hyperhomocysteinemia
Thrombotic
Prph2-related Disorder
Alcohol Consumption (drinks Per Week) (mtag)
Argininosuccinate Lyase Deficiency
Concentration of Small Vldl Particles
Charcot-marie-tooth Disease Axonal Type 2s
Common Executive Function
Direct Bilirubin Levels
Facial Appearance
Pkhd1-related Disorder
Autosomal Recessive Congenital Ichthyosis 1
Graves' Disease
Aspartate Aminotransferase to Alanine Aminotransferase Ratio
Autosomal Recessive Nonsyndromic Hearing Loss 9
Developmental Delay
Hereditary Insensitivity to Pain with Anhidrosis
Hypogonadotropic Hypogonadism 2 with or Without Anosmia
Noonan Syndrome and Noonan-related Syndrome
Pkd1-related Disorder
Jt Interval
Mitochondrial Complex Iv Deficiency
Selective
Hand Grip Strength
Maple Syrup Urine Disease Type 1a
Positive Affect
Type Iii
Pmm2-congenital Disorder of Glycosylation
Sex Hormone-binding Globulin Levels and Heel Estimated Bone Mineral Density
Angelman Syndrome
Axonal
Blood Cell Traits Latent Factor 8 (white Cell)
Distal Myopathy with Anterior Tibial Onset
Angelman Syndrome-like
Familial Hemophagocytic Lymphohistiocytosis 3
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