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)
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2i
Bardet-biedl Syndrome 4
Cholesterol to Total Lipids in Large Vldl Percentage
Cleft Lip with or Without Cleft Palate
Congenital Disorder of Deglycosylation
Cryopyrin Associated Periodic Syndrome
Gut Microbial Network Clusters (cyan (at 3 Months) X Any Breastfeeding (3 Months) Interaction
Hyperammonemia
Jervell and Lange-nielsen Syndrome 1
Megalencephalic Leukoencephalopathy with Subcortical Cysts 1
Osteogenesis Imperfecta Type Iii
Pelizaeus-merzbacher Disease
Phospholipids in Small Ldl
Phospholipids to Total Lipids Ratio in Large Ldl
Platelet Count During Third Trimester of Pregnancy
Respiratory Diseases
Sphingomyelin(39:1)_[m+h]1+ Levels
Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency Type A
Allergic Rhinitis
Blepharophimosis
Free Cholesterol to Total Lipids in Idl Percentage
Household Income
Lymphoma
Monogenic Hearing Loss
Nonatopic Asthma
Peroxisome Biogenesis Disorder 3a (zellweger)
Pole-related Disorder
Sbbys Type
Susceptibility to Mononeuropathy of the Median Nerve
Thrombophilia Due to Protein C Deficiency
Vertigo
Waist Circumference Adjusted For Bmi in Active Individuals
White Blood Cell Count (basophil)
6-pyruvoyl-tetrahydrobiopterin Synthase Deficiency
Alzheimer's Disease, Proxy Alzheimer's Disease or Related Dementias in Apoe E4 Non-carriers
Blood Urea Nitrogen (bun, Minimum, Inv-norm Transformed)
Carney Complex
Cblb Type
Cholesterol in Large Vldl
Cholesterol to Total Lipids Ratio in Large Hdl
Coronary Artery Disease or Fibrinogen Levels (pleiotropy)
Dilated Cardiomyopathy 1jj
Familial Cold Autoinflammatory Syndrome 2
Hereditary Antithrombin Deficiency
Hereditary Spastic Paraplegia 49
Leukocyte Adhesion Deficiency 1
Mdga1 Protein Levels
Melnick-fraser Syndrome
Multisite Chronic Pain
Nephronophthisis 3
Parkinson's Disease or First Degree Relation to Individual with Parkinson's Disease
Peroxisome Biogenesis Disorder 2b
Primary Congenital
Rheumatoid Arthritis or Type 1 Diabetes
Rs-6-hydroxywarfarin Levels
Systolic Blood Pressure X Alcohol Consumption Interaction (2df Test)
Ventricular Fibrillation
Vertical Cup-disc Ratio (multi-trait Analysis)
Woolly Hair-skin Fragility Syndrome
Adrenal Hypoplasia Congenita
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