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)
Aggressive Behavior
Aging (facial)
Agnathia-otocephaly Complex
Agrin Levels
Agrn/btn2a1 Protein Level Ratio
Ahcy/fabp5 Protein Level Ratio
Aica-ribosiduria
Aifm1 Protein Levels
Aimp1-related Disorder
Airway Obstruction (fev1/fvc<lower Limit of Normal) in Never Smokers
Akt2-related Disorder
Akt3 Protein Levels
Alas2-related Disorder
Alcam/notch1 Protein Level Ratio
Alcohol Frequency Weekly (weighted Gwa)
Aldh1a1/pklr Protein Level Ratio
Aldh3a2-related Disorder
Aldoa-related Disorder
Aldosterone Producing Adenoma
Alg6-related Disorder
Alkaline Ceramidase 3 Deficiency
Alkenylphosphatidylcholine (p-15:0/20:4) (b) Levels
Alkenylphosphatidylcholine (p-16:0/18:0) Levels
Alkenylphosphatidylethanolamine (p-17:0/20:4) (a) Levels
Alkenylphosphatidylethanolamine (p-18:1/18:2) (b) Levels
Alkenylphosphatidylethanolamine (p-20:0/22:6) Levels
Alkylphosphatidylcholine (o-16:0/16:0) Levels
Alkylphosphatidylcholine (o-16:0/22:6) Levels
Alkylphosphatidylcholine (o-18:0/20:4) Levels
Alkylphosphatidylcholine (o-34:1) Levels
Alkylphosphatidylcholine (o-38:5) Levels
Alkylphosphatidylcholine (o-40:5) Levels
Allergen Component Sensitization (mercurialis Annua 1)
Alpha- and Gamma-adaptin-binding Protein P34 Levels
Alpha-1,3-mannosyl-glycoprotein 4-beta-n-acetylglucosaminyltransferase A Levels
Alpha-1,3-mannosyl-glycoprotein 4-beta-n-acetylglucosaminyltransferase C Levels
Alpha-1,6-mannosyl-glycoprotein 2-beta-n-acetylglucosaminyltransferase Levels
Alpha-2-antiplasmin Levels
Alpha-2-macroglobulin Receptor-associated Protein Levels (lrpap1.3640.14.3)
Als2-related Motor Neuron Disease
Altered
Alx4 Protein Levels
Ambp/hyou1 Protein Level Ratio
Amed Syndrome
Amelogenesis Imperfecta Hypomaturation Type 2a5
Amelogenesis Imperfecta Type 1f
Aminopeptidase B Levels
Amorph Type
Amsh-like Protease Levels
Amyloid Beta A4 Precursor Protein-binding Family B Member 2 Levels
Amyloid Beta Positivity
Amyotrophic Lateral Sclerosis in C9orf72 Mutation Negative Individuals
Amyotrophic Lateral Sclerosis Type 23
Anaphylactic Shock Nos (phecode 946)
And Adult-onset Progressive Leukoencephalopathy
And Ataxia
And Attention Deficit-hyperactivity Disorder
And Autonomic Dysfunction
And Joint Dislocations
And Lissencephaly
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →