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)
Basal Cell Carcinoma (mtag)
72 variants Cancer
Cantagrel Type
72 variants Other
Charcot-marie-tooth Disease Type 4f
72 variants Other
Cholesterol to Total Lipids Ratio in Small Hdl
72 variants Metabolic
Cockayne Syndrome Type 1
72 variants Other
Coronary Artery Disease (myocardial Infarction, Percutaneous Transluminal Coronary Angioplasty, Coronary Artery Bypass Grafting, Angina or Chromic Ischemic Heart Disease)
72 variants Cardiovascular
Covid-19 (covid Pneumonia Vs Population)
72 variants Other
Crisp2 Protein Levels
72 variants Other
Deficiency of Malonyl-coa Decarboxylase
72 variants Other
Developmental Disorder
72 variants Other
Femur Total Bone Mineral Density X Gut Microbiota (genus Lactococcus) Interaction
72 variants Other
Fetal Akinesia Deformation Sequence 3
72 variants Other
Gut Microbial Network Clusters (tan (at 3 Months) X Summer Birth (jun-aug) Interaction
72 variants Other
Homocystinuria
72 variants Other
Intraocular Pressure (confirmatory Factor Analysis Factor 26)
72 variants Other
Klk1 Protein Levels
72 variants Other
Leber Congenital Amaurosis 3
72 variants Other
Leukoencephalopathy
72 variants Other
Neutrophil Side Scatter
72 variants Other
Phosphatidylcholine(33:3)_[m+h]1+/phosphatidylethanolamine(36:3)_[m+h]1+/phosphatidate(38:4)_[m+nh4]1+ Levels
72 variants Other
Phosphatidylcholine(38:4)_[m+oac]1-/phosphatidylserine(42:3)_[m-h]1- Levels
72 variants Other
Pili Torti-deafness Syndrome
72 variants Other
Platelet Side Fluorescence
72 variants Hematologic
Psoriatic Arthritis
72 variants Musculoskeletal
Pulmonary
72 variants Respiratory
Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic Manifestations
72 variants Ophthalmic
Retinitis Pigmentosa 45
72 variants Other
S-warfarin to R-warfarin Ratio
72 variants Pharmacogenomic
Surfactant Metabolism Dysfunction
72 variants Pharmacogenomic
Venous Thromboembolism (snp X Snp Interaction)
72 variants Other
Wfdc12 Protein Levels
72 variants Other
Age At Peak Height Velocity
71 variants Other
Autosomal Recessive Limb-girdle Muscular Dystrophy Type R18
71 variants Other
Bicarbonate (maximum, Inv-norm Transformed)
71 variants Other
Brachyolmia-amelogenesis Imperfecta Syndrome
71 variants Other
Carnitine Acylcarnitine Translocase Deficiency
71 variants Other
Carpal Tunnel Syndrome
71 variants Other
Cholelithiasis
71 variants Other
Cholesterol Levels in Small Vldl
71 variants Metabolic
Cholesteryl Esters to Total Lipids in Large Ldl Percentage
71 variants Metabolic
Col2a1 Protein Levels
71 variants Other
Dilated Cardiomyopathy 1w
71 variants Other
Feeling Worry
71 variants Other
Frontotemporal Dementia And/or Amyotrophic Lateral Sclerosis 4
71 variants Neurological
Glucose Homeostasis Traits
71 variants Other
Hyperlipidemia (phecode 272.1)
71 variants Metabolic
Ischemic Stroke (cardioembolic)
71 variants Cardiovascular
Klb Protein Levels
71 variants Other
Lesch-nyhan Syndrome
71 variants Other
Male Infertility with Azoospermia or Oligozoospermia Due to Single Gene Mutation
71 variants Other
Methylmalonic Aciduria and Homocystinuria Type Cbld
71 variants Other
Microangiopathy and Leukoencephalopathy
71 variants Other
Noonan Syndrome 10
71 variants Other
Nphp4-related Disorder
71 variants Other
Peripheral Neuropathy
71 variants Neurological
Phosphatidylcholine-o(38:5)_[m+h]1+/phosphatidylcholine-p(38:4)_[m+h]1+ Levels
71 variants Other
Phosphatidylcholine(37:4)_[m+h]1+/phosphatidylethanolamine(40:4)_[m+h]1+/phosphatidate(42:5)_[m+nh4]1+ Levels
71 variants Other
Pontine
71 variants Other
Ptch1-related Disorder
71 variants Other
Renal Tubular Dysgenesis of Genetic Origin
71 variants Renal
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