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)
Noonan Syndrome 6
Npc2 Protein Levels
Number of Non-cancer Illnesses (standard Gwa)
Obsessive-compulsive Traits
Obstetric Antiphospholipid Syndrome
Octadecadienedioate (c18:2-dc) Levels
Odontochondrodysplasia 1
Ofd1-related Disorder
Osteonecrosis in Systemic Lupus Erythematosus
Ovarian Hyperstimulation Syndrome
P-selectin Glycoprotein Ligand 1 Levels
Pachyonychia Congenita 1
Palmoplantar Pustulosis
Paroxysmal Nocturnal Hemoglobinuria 1
Paroxysmal Nonkinesigenic Dyskinesia 1
Pediatric Areal Bone Mineral Density (radius)
Pediatric Bone Mineral Content (hip)
Pediatric Bone Mineral Density (spine)
Percent Liver Fat
Percentage Gas Trapping
Periodontal Disease-related Phenotype (socransky)
Periodontal Microbiota
Periodontitis / Loose Teeth (mtag)
Peritoneal or Intestinal Adhesions (phecode 560.3)
Peroxisome Biogenesis Disorder 10a (zellweger)
Pex7-related Disorder
Phkb-related Disorder
Phosphatidylcholine (15:0_18:2) Levels
Phosphatidylcholine (18:1_20:4) Levels
Phosphatidylcholine_36:5_[m+h]1+/phosphatidylethanolamine_39:5_[m+h]1+/phosphatidate_41:6_[m+nh4]1+ Levels
Phosphatidylcholine_52:4_[m+oac]1- Levels
Phosphatidylcholine-o_35:4_[m+oac]1-/phosphatidylcholine-p_35:3_[m+oac]1- Levels
Phosphatidylcholine-o_38:4_[m+h]1+/phosphatidylcholine-p_38:3_[m+h]1+ Levels
Phosphatidylcholine-o_40:6_[m+h]1+/phosphatidylcholine-p_40:5_[m+h]1+ Levels
Phosphatidylethanolamine (15-mhda_18:2) Levels
Phosphatidylethanolamine (18:0_20:3) (a) Levels
Phosphatidylethanolamine (18:1_18:2) Levels
Phosphatidylethanolamine-o_40:6_[m-h]1-/phosphatidylethanolamine-p_40:5_[m-h]1- Levels
Phosphatidylglycerol_36:0_[m-h]1- Levels
Phosphatidylinositol (18:0_20:2) Levels
Phosphatidylserine-p_42:1_[m+h]1+/phosphatidylglycerol-p_42:6_[m+nh4]1+ Levels
Physiological Traits
Pituitary Hyperfunction (phecode 253.1)
Plasma Clusterin Levels
Plasma Omega-3 Fatty Acids (% of Total Fa) From Nmr X Dietary Omega-3 Fatty Acid Intake Interaction
Platelet-type Bleeding Disorder 16
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 2
Polyneuropathy in Diabetes (phecode 250.6)
Pomc Protein Levels
Pontocerebellar Hypoplasia Type 3
Portal Hypertension
Positive Urgency (measured By Upps At 28 Years)
Post-traumatic Stress Disorder (asjusted For Relatedness)
Pretibial Dystrophic Epidermolysis Bullosa
Primary Ciliary Dyskinesia 17
Primary Ciliary Dyskinesia 18
Primary Ciliary Dyskinesia 2
Primary Ciliary Dyskinesia 22
Primary Microcephaly
Proline Levels
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