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)
Psapl1 Protein Levels
Ratio of Polyunsaturated Fatty Acids to Total Fatty Acids
Syndromic X-linked Intellectual Disability Claes-jensen Type
Van Maldergem Syndrome 2
9 Conditions
Autosomal Dominant Nonsyndromic Hearing Loss 4a
Budd-chiari Syndrome
Camptomelic Dysplasia
Cdsn Protein Levels
Ceacam21 Protein Levels
Cerebral Cavernous Malformation 2
Cholesteryl Ester Levels in Small Vldl
Cholesteryl Ester(18:3)_[m+nh4]1+ Levels
Combined Oxidative Phosphorylation Defect Type 17
Covid-19 (critical Illness Vs Population)
Covid-19 (severe Vs Non-severe with Positive Test)
Dent Disease Type 1
Ease of Getting Up in the Morning
Familial Hemophagocytic Lymphohistiocytosis
Freeman-sheldon Syndrome
Male Infertility
Psg1 Protein Levels
Retinitis Pigmentosa 1
Senior-loken Syndrome 5
Senior-loken Syndrome 7
Serpini2 Protein Levels
Sftpd Protein Levels
Smith-magenis Syndrome
Total Concentration of Branched-chain Amino Acids (leucine + Isoleucine + Valine)
Triglyceride Levels in Very Large Hdl
Walking Pace
Weill-marchesani 4 Syndrome
Allergen Component Sensitization (ambrosia Artemisiifolia 1)
Anophthalmia/microphthalmia-esophageal Atresia Syndrome
Brugada Syndrome 5
Bst1 Protein Levels
Cardio-facio-cutaneous Syndrome
Cholesteryl Esters in Small Vldl
Clps Protein Levels
Ddx41-related Hematologic Malignancy Predisposition Syndrome
Hennekam Lymphangiectasia-lymphedema Syndrome 2
Hyperphosphatemic
Lactic Acidosis
Ldl X Depression Interaction (2df Test)
Man2b2 Protein Levels
Nonsyndromic
Osteogenesis Imperfecta Type 7
Paroxysmal Extreme Pain Disorder
Pontocerebellar Hypoplasia
Ratio of Polyunsaturated Fatty Acids to Monounsaturated Fatty Acids
Recurrent
Snoring
Tnn Protein Levels
X-11315 Levels
Alpp Protein Levels
Amelogenesis Imperfecta
Autosomal Recessive Hypophosphatemic Bone Disease
Autosomal Recessive Nonsyndromic Hearing Loss 37
Bone Mineral Density (hip)
Calcium (maximum, Inv-norm Transformed)
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