Health Conditions

43,676 conditions with known genetic associations in our database.

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