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)
Gc Protein Levels
Hereditary Acrodermatitis Enteropathica
Hereditary Spastic Paraplegia 8
Hypohidrotic/hair/nail Type
Il1rap Protein Levels
Ldl Cholesterol Levels X Long Total Sleep Time Interaction (2df Test)
Leber Congenital Amaurosis 9
Mean Volume of Bilateral Amygdala
Methylcrotonyl-coa Carboxylase Deficiency
Mitochondrial Complex V (atp Synthase) Deficiency
Mln Protein Levels
Motor Premotor Area
Nail-patella Syndrome
Neonatal Diabetes Mellitus
Neuroticism Conditioned On Average Household Income Before Tax (multi-trait Conditioning and Joint Analysis)
Nuclear Type 4
Oculodentodigital Dysplasia
Opioid Use Disorder (mtag)
Other Chronic Ischemic Heart Disease, Unspecified (phecode 411.8)
Parental Longevity (combined Parental Age At Death)
Phosphate Levels (ukb Data Field 30810)
Plantar Warts
Platelet Forward Scatter
Polymerase Proofreading-related Adenomatous Polyposis
Primary Ciliary Dyskinesia 28
Ratio of Omega-3 Fatty Acids to Total Fatty Acids
S-6-hydroxywarfarin to S-warfarin Ratio
Schaaf-yang Syndrome
Sideroblastic Anemia 2
Siglec6 Protein Levels
Spink4 Protein Levels
Thiazide-induced Adverse Metabolic Effects in Hypertensive Patients
Timd4 Protein Levels
Total Cholesterol Levels in Ldl
Total Lipids in Large Hdl (ukb Data Field 23559)
Urinary Sodium Excretion
White Matter Hyperintensity Volume (adjusted For Hypertension)
X-linked Lymphoproliferative Disease Due to Xiap Deficiency
3-hydroxy-3-methylglutaryl-coa Synthase Deficiency
3-methylglutaconic Aciduria
8q24.3 Microdeletion Syndrome
Alagille Syndrome Due to A Notch2 Point Mutation
Allan-herndon-dudley Syndrome
Alternating Hemiplegia of Childhood 2
Autosomal Recessive Congenital Ichthyosis 3
Basophil Percentage of Granulocytes
Bosch-boonstra-schaaf Optic Atrophy Syndrome
Capillary Malformation-arteriovenous Malformation 1
Carotid Intima-media Thickness (mtag)
Cd200r1 Protein Levels
Cd70 Protein Levels
Cdh23-related Disorder
Cognitive Function (generalized Correlation Coefficient)
Combined Deficiency Of
Cone-rod Dystrophy 15
Congenital Generalized Lipodystrophy Type 2
Cr2 Protein Levels
Developmental Cataract
Diastolic Blood Pressure X Smoking Status (current Vs Non-current) Interaction (2df Test)
Dxa-bone Mineral Density (total Body) (ukb Data Field 23236)
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