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)
Nuclear Type 18
12 variants Other
Nuclear Type 23
12 variants Other
Nxph3 Protein Levels
12 variants Other
Ocular Albinism with Congenital Sensorineural Hearing Loss
12 variants Other
Oleoyl-oleoyl-glycerol (18:1/18:1) [1] Levels in Elite Athletes
12 variants Other
Olr1 Protein Levels
12 variants Other
Optic Atrophy 12
12 variants Other
Oral Lichen Planus
12 variants Other
Orotidine Levels
12 variants Other
Osteootohepatoenteric Syndrome
12 variants Other
Other Specified Disorders of Plasma Protein Metabolism (phecode 270.38)
12 variants Pharmacogenomic
P-selectin Levels
12 variants Other
Pachyonychia Congenita 2
12 variants Other
Pag1 Protein Levels
12 variants Other
Palmitic Acid (16:0) Levels
12 variants Other
Pancreatic Ductal Adenocarcinoma
12 variants Cancer
Pancreatitis
12 variants Gastrointestinal
Paracentral Lobule Volume
12 variants Other
Parkinson Disease 17
12 variants Neurological
Pdcd5 Protein Levels
12 variants Other
Pdgfa/serpine1 Protein Level Ratio
12 variants Other
Pediatric Bone Mineral Content (femoral Neck)
12 variants Other
Perceived Intensity of Neohesperidin Dihydrochalcone
12 variants Other
Pericardial Fat (model 1)
12 variants Other
Permanent Neonatal Diabetes Mellitus-pancreatic and Cerebellar Agenesis Syndrome
12 variants Metabolic
Pex12-related Disorder
12 variants Other
Phosphatidate_34:2_[m-h]1- Levels
12 variants Other
Phosphatidylcholine (14:0_18:2) Levels
12 variants Other
Phosphatidylcholine (16:0_22:5) Levels
12 variants Other
Phosphatidylcholine (16:1_18:1) Levels
12 variants Other
Phosphatidylcholine (18:1_18:1) Levels
12 variants Other
Phosphatidylcholines (37:4) Levels
12 variants Other
Phosphatidylethanolamine (16:0_22:6) Levels
12 variants Other
Phosphatidylethanolamine (16:1_18:2) Levels
12 variants Other
Phosphatidylethanolamine (17:0_20:4) Levels
12 variants Other
Phosphatidylinositol (18:0_20:3) Levels
12 variants Other
Phosphatidylinositol_40:6_[m-h]1- Levels
12 variants Other
Phosphatidylinositol(34:0)_[m-h]1- Levels
12 variants Other
Physical Activity
12 variants Other
Pilarowski-bjornsson Syndrome
12 variants Other
Pituitary Stalk Interruption Syndrome
12 variants Other
Pitx2-related Eye Abnormalities
12 variants Ophthalmic
Plasma Copper Levels
12 variants Other
Plasma Titanium Levels
12 variants Other
Plasma Trimethylamine N-oxide Levels
12 variants Other
Platelet Response to Aspirin
12 variants Hematologic
Plexin-b2 Levels
12 variants Other
Plod1-related Disorder
12 variants Other
Pnpt1-related Disorder
12 variants Other
Polr-related Leukodystrophy
12 variants Other
Poor Response To
12 variants Other
Porencephaly-microcephaly-bilateral Congenital Cataract Syndrome
12 variants Other
Porphobilinogen Synthase Deficiency
12 variants Other
Ppcdc Protein Levels
12 variants Other
Pre Bronchodilator Fev1
12 variants Other
Pre Bronchodilator Fev1/fvc Ratio
12 variants Other
Primary Ciliary Dyskinesia 24
12 variants Dermatologic
Primary/intrinsic Cardiomyopathies (phecode 425.1)
12 variants Other
Prkag2-related Disorder
12 variants Other
Progesterone Levels
12 variants Other
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