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)
X-24812 Levels
X-linked 30
Xdh-related Disorder
Zfyve19 Protein Levels
1-methylurate Levels
1-stearoyl-gpe (18:0) Levels
2-aminooctanoate Levels
2-naphthol Sulfate Levels
3beta-hydroxy-5-cholestenoate Levels
5-dodecenoylcarnitine (c12:1) Levels
5alpha-pregnan-3beta,20alpha-diol Disulfate Levels
Abortive Cerebellar Ataxia
Academic Attainment (english)
Ace2 Protein Levels
Acvrl1 Protein Levels
Acvrl1-related Disorder
Adam9 Protein Levels
Adamtsl4-related Disorder
Adiponectin Levels (bmi-adjusted)
Adult-onset Proximal Spinal Muscular Atrophy
Adverse Response to Inhaled Corticosteroid Treatment X Age Interaction in Asthma
Alanine Aminotransferase Levels in Low Alcohol Consumption
Amyotrophic Lateral Sclerosis Type 8
And Dysequilibrium Syndrome 2
And Fanconi-type Renal Dysfunction
And Hypotonia
And Limb Abnormalities
And Premature Immunosenescence Associated with Tripeptidyl-peptidase Ii Deficiency
And Variable Brain Anomalies
Angptl2 Protein Levels
Apoa2 Protein Levels
Apod Protein Levels
Apof Protein Levels
Apolipoprotein B Levels X Vegetarianism Interaction
Arrhinia with Choanal Atresia and Microphthalmia Syndrome
Arthralgia/ankylosis of Temporomandibular Joint (phecode 526.42)
Atp13a2-related Disorder
Atp1a3-related Disorder
Atrial Septal Defect 2
Attention Deficit Hyperactivity Disorder or Cannabis Use
Autosomal Dominant Nonsyndromic Hearing Loss 3b
Autosomal Recessive 18
Autosomal Recessive Nonsyndromic Hearing Loss 79
Autosomal Recessive Osteopetrosis 5
B-cell Lymphoblastic Leukemia or Inflammatory Bowel Disease (pleiotropy)
B-cell Telomere Length
Bcan Protein Levels
Bcat1 Protein Levels
Beta-citrylglutamate Levels
Bilateral Perisylvian
Biochemical Measures
Bipolar Disorder with Mood-incongruent Psychosis
Blepharophimosis-impaired Intellectual Development Syndrome
Body Fat Percentage or Coronary Artery Disease (mtag)
Body Mass Index (adult)
Bone Mineral Density (paediatric, Total Body Less Head)
Bone Ultrasound Measurement (velocity of Sound)
Brain Amyloid Deposition (pet Imaging)
Branched-chain, Straight-chain, or Cyclopropyl 12:1 Fatty Acid Levels
Brat1-related Disorder
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →