Health Conditions

43,676 conditions with known genetic associations in our database.

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