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)
Plxnb2 Protein Levels
Popliteal Pterygium Syndrome
Porencephaly 2
Prr4 Protein Levels
Shingles
Spag1 Protein Levels
Tall Stature-scoliosis-macrodactyly of the Great Toes Syndrome
Triglyceride Levels X Alcohol Consumption (drinkers Vs Non-drinkers) Interaction (2df)
Vascular Endothelial Function
Alcohol Use Disorder (mtag)
Autosomal Dominant 29
Autosomal Recessive 2
Axenfeld-rieger Syndrome Type 1
Bohring-opitz Syndrome
Bpifb1 Protein Levels
Cholesteryl Ester Levels in Vldl
Cholesteryl Esters in Large Ldl
Col4a4-related Disorder
Dbh Protein Levels
De Sanctis-cacchione Syndrome
Desmoid Disease
Facial Morphology (profile Nasal Angle)
Familial Hypertrophic 27
Glycogen Storage Disease Ixc
Icd10 D25: Leiomyoma of Uterus
Left Ventricular Noncompaction Cardiomyopathy
Mendelian Susceptibility to Mycobacterial Diseases Due to Partial Stat1 Deficiency
Neutrophil (fraction, Maximum, Inv-norm Transformed)
Pdgfrb Protein Levels
Pglyrp2 Protein Levels
Phosphatidylcholine(32:0)_[m+h]1+/phosphatidylethanolamine(35:0)_[m+h]1+/phosphatidate(37:1)_[m+nh4]1+ Levels
Piebaldism
Pilra Protein Levels
Potassium (maximum, Inv-norm Transformed)
Prss53 Protein Levels
Rothmund-thomson Syndrome Type 2
Sncg Protein Levels
Stable Angina Pectoris
Stargardt Disease 4
Tdgf1 Protein Levels
Tsc1-related Disorder
With Psychomotor Retardation and Characteristic Facies 3
Adenine Phosphoribosyltransferase Deficiency
Angina Pectoris
Blood Cell Traits Latent Factor 1 (white Cell)
Bone Mineral Density
Cardioencephalomyopathy
Cholesteryl Ester Levels in Very Small Vldl
Dilated Cardiomyopathy 1j
Fatal Infantile
Fgfbp2 Protein Levels
Gut Microbial Network Clusters (pink (at 1 Year) X Any Breastfeeding (duration) Interaction
Hereditary Spastic Paraplegia 31
Hyperekplexia 3
Hypertrophic Cardiomyopathy 20
Il5ra Protein Levels
Immunodeficiency 23
Intrinsic Epigenetic Age Acceleration
Left Ventricular Noncompaction 8
Lilrb2 Protein Levels
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