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)
Acute Laryngitis and Tracheitis (phecode 465.4)
13 variants Other
Adamtsl4 Protein Levels
13 variants Other
Adult-onset Citrullinemia Type I
13 variants Other
Advanced Glycosylation End Product-specific Receptor, Soluble Levels
13 variants Other
Aff4-related Disorder
13 variants Other
Age At Natural Menopause or Uterine Leiomyomata (pleiotropy)
13 variants Other
Akap9-related Disorder
13 variants Other
Ambidextrousness (ambidextrous Vs Right-handed)
13 variants Other
Amyotrophic Lateral Sclerosis Type 21
13 variants Other
And Brain Atrophy
13 variants Other
And Gait Abnormalities
13 variants Other
And Pseudo-pelger-huet Anomaly
13 variants Other
And/or Spastic Paraplegia
13 variants Other
Angiopoietin-1 Receptor Levels
13 variants Other
Angptl3 Protein Levels
13 variants Other
Ank3-related Disorder
13 variants Other
Apolipoprotein C-iii Levels
13 variants Other
App/pdgfa Protein Level Ratio
13 variants Other
Arachidonic Acid Levels
13 variants Other
Arsa-related Disorder
13 variants Other
Arthropathy Associated with Other Disorders (phecode 713)
13 variants Other
Asrgl1 Protein Levels
13 variants Other
Atp7a-related Disorder
13 variants Other
Autosomal Dominant 38
13 variants Other
Autosomal Dominant 71
13 variants Other
Autosomal Dominant 72
13 variants Other
Autosomal Dominant Robinow Syndrome 3
13 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 15
13 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 36
13 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 76
13 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 86
13 variants Other
Autosomal Recessive Nonsyndromic Hearing Loss 98
13 variants Other
Autosomal Recessive Osteopetrosis 2
13 variants Other
Axial Spondylometaphyseal Dysplasia
13 variants Other
Axin1/nfatc1 Protein Level Ratio
13 variants Other
Bacteremia
13 variants Other
Behcet Disease
13 variants Other
Blood Cell Traits Latent Factor 20 (red Cell)
13 variants Other
Branched-chain Keto Acid Dehydrogenase Kinase Deficiency
13 variants Other
C-c Motif Chemokine 18 Levels
13 variants Other
C8g Protein Levels
13 variants Other
C9 Protein Levels
13 variants Other
Cadherin-5 Levels
13 variants Other
Calca Protein Levels
13 variants Other
Carbonic Anhydrase 6 Levels
13 variants Other
Cardiofaciocutaneous Syndrome 2
13 variants Other
Carotid Plaque Maximum Area
13 variants Other
Cataract 16 Multiple Types
13 variants Other
Cataract 22 Multiple Types
13 variants Other
Ccdc80 Protein Levels
13 variants Other
Cd164 Protein Levels
13 variants Other
Cd6 Levels
13 variants Other
Cdkn1a Protein Levels
13 variants Other
Cdkn2d/tacc3 Protein Level Ratio
13 variants Other
Cdon Protein Levels
13 variants Other
Cerebrospinal Fluid T-tau Levels
13 variants Other
Cerebrovascular Disease (phecode 433)
13 variants Other
Cerotoylcarnitine (c26) Levels
13 variants Other
Cfh Protein Levels
13 variants Other
Cfhr5 Deficiency
13 variants Other
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