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)
Atp5if1/decr1 Protein Level Ratio
Atp5if1/fis1 Protein Level Ratio
Atp5if1/fxn Protein Level Ratio
Atp5if1/hspa1a Protein Level Ratio
Atp5if1/manf Protein Level Ratio
Atp5if1/skap2 Protein Level Ratio
Atp5if1/snap29 Protein Level Ratio
Atrial Natriuretic Factor Levels
Atrial Septal Defect 8
Atrioventricular Block
Atrioventricular Block, Complete (phecode 426.24)
Atrophic Gastritis
Atrophy of Edentulous Alveolar Ridge (phecode 525.2)
Attention Deficit Hyperactivity Disorder (phecode 313.1)
Attention Deficit Hyperactivity Disorder and Autism Spectrum Disorder
Attention Deficit Hyperactivity Disorder or Putamen Volume (pleiotropy)
Attenuated
Attenuated Frontometaphyseal Dysplasia
Atxn1-related Disorder
Atxn10/casp10 Protein Level Ratio
Atxn2-related Disorder
Atxn7-related Disorder
Atypical Nephropathic
Auc of Atorvastatin
Aural Atresia
Auriculocondylar Syndrome 3
Aurora Kinase A Levels
Autism Spectrum Disorder in Attention Deficit Hyperactivity Disorder
Autoimmune Hepatitis
Autoimmune Polyglandular Syndrome Type 1
Autoimmune Pulmonary Alveolar Proteinosis
Autoimmune Thrombocytopenia
Autoinflammation with Arthritis and Dyskeratosis
Autoinflammation with Arthritis and Vasculitis
Autoinflammation with Episodic Fever and Immune Dysregulation
Autosomal Dominant 85
Autosomal Dominant and Autosomal Recessive Mfn2-related Disorders
Autosomal Dominant Charcot-marie-tooth Disease Type 2k
Autosomal Dominant Kat6b-related Disorders
Autosomal Dominant Nonsyndromic Hearing Loss 28
Autosomal Dominant Nonsyndromic Hearing Loss 33
Autosomal Dominant Nonsyndromic Hearing Loss 40
Autosomal Dominant Nonsyndromic Hearing Loss 44
Autosomal Dominant Nonsyndromic Hearing Loss 50
Autosomal Dominant Nonsyndromic Hearing Loss 69
Autosomal Dominant Nonsyndromic Sensorineural 39
Autosomal Dominant Omodysplasia
Autosomal Dominant Opitz G/bbb Syndrome
Autosomal Dominant Rhegmatogenous Retinal Detachment
Autosomal Dominant Sideroblastic Anemia
Autosomal Recessive 122
Autosomal Recessive 22
Autosomal Recessive 30
Autosomal Recessive 45
Autosomal Recessive 50
Autosomal Recessive 52
Autosomal Recessive 56
Autosomal Recessive 59
Autosomal Recessive 73
Autosomal Recessive 76
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