Health Conditions
43,676 conditions with known genetic associations in our database.
All(43,676)
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)
Adult Hypophosphatasia
Beckwith-wiedemann Syndrome
Concentration of Hdl Particles
Neurodevelopmental Disorder with Hypotonia
Tinnitus
Triglycerides in Small Vldl
Usher Syndrome Type 1b
Type 6
Wiedemann-steiner Syndrome
Cholesteryl Esters in Hdl
Greig Cephalopolysyndactyly Syndrome
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2o
Autosomal Recessive Osteopetrosis 1
Basophil Percentage of White Cells
Cholesteryl Ester Levels in Chylomicrons and Extremely Large Vldl
Congenital Myasthenic Syndrome
Glut1 Deficiency Syndrome 1
Granulocyte Percentage of Myeloid White Cells
Mhc Class Ii Deficiency
Trunk Fat Mass (ukb Data Field 23128)
Cockayne Syndrome Type 2
Familial Thoracic 7
Holocarboxylase Synthetase Deficiency
Type Ib
Triglycerides in Very Small Vldl
Type B3
Eosinophil (absolute Count, Maximum, Inv-norm Transformed)
Triglyceride Levels in Chylomicrons and Extremely Large Vldl
Alcohol Consumption (drinks Per Week)
Income (mtag)
Alport Syndrome 3b
Autosomal Recessive Dopa Responsive Dystonia
Creatinine (mean, Inv-norm Transformed)
Hypohidrotic X-linked Ectodermal Dysplasia
Rubinstein-taybi Syndrome Due to Ep300 Haploinsufficiency
Tip-toe Gait
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2l
Cerebrospinal Fluid Strem-2 Levels
Predicted Visceral Adipose Tissue
Atm-related Disorder
Cerebellar Grey Matter Morphology (mostest)
Classic Homocystinuria
Cone-rod Dystrophy 3
Gnathodiaphyseal Dysplasia
Joubert Syndrome 17
Deficiency of Acetyl-coa Acetyltransferase
Focal Segmental Glomerulosclerosis 5
Monocyte (fraction, Maximum, Inv-norm Transformed)
Bardet-biedl Syndrome 1
Dilated Cardiomyopathy 1aa
Irido-corneo-trabecular Dysgenesis
Metaphyseal Chondrodysplasia
3-methylcrotonyl-coa Carboxylase 1 Deficiency
Acute Febrile Neutrophilic Dermatosis
Arrhythmogenic Right Ventricular Dysplasia 2
Total Body Bone Mineral Density
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2k
Total Cholines Levels
Whole Brain Free Water Diffusion (multivariate Analysis)
Carnitine Palmitoyltransferase Ii Deficiency
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