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)
Prothrombin Time
Psat Deficiency
Psoriatic Arthropathy (phecode 696.42)
Pulmonary Tuberculosis
Purpura and Other Hemorrhagic Conditions (phecode 287)
Pygm-related Disorder
Rbm20-related Disorder
Regional Cortical Thickness (inferiorparietal)
Relt Protein Levels
Remission After Antidepressant Treatment in Major Depressive Disorder
Response to Antipsychotic Therapy (extrapyramidal Side Effects)
Response to Citalopram Treatment
Response to Methotrexate in Juvenile Idiopathic Arthritis
Retinal Dystrophy with or Without Macular Staphyloma
Retinal Thickness (functional Principal Component 6)
Revision Surgery After Total Joint Arthroplasty
Right Unilateral Cleft Lip
Rnase3 Protein Levels
Rolandic Epilepsy
Rp1l1-related Disorder
Rspo1 Protein Levels
S-adenosylhomocysteine (sah) Levels
S-methylcysteine Levels
Samd9-related Disorder
Scara5 Protein Levels
Sdk2 Protein Levels
Seasonality and Depression
Sema3f Protein Levels
Sensory Peripheral Neuropathy in Microtubule Targeting Agent-treated Breast Cancer
Seropositivity For Lactobacillus Phage Lfeinf Peptide (twist_64023)
Seropositivity For Lactobacillus Phage Lfeinf Peptide (twist_88894)
Seropositivity For Streptococcus Pneumoniae Peptide (agilent_229757)
Seropositivity For Streptococcus Pyogenes Peptide (agilent_235068)
Serum Neurofilament Light Levels
Serum Polyunsaturated Fatty Acid Concentration X Mediterranean Diet Adherence Interaction in Metabolic Syndrome
Severe Combined Immunodeficiency Due to Carmil2 Deficiency
Sialic Acid-binding Ig-like Lectin 6 Levels
Slc39a5 Protein Levels
Slitrk2 Protein Levels
Slx4-related Disorder
Smarcal1-related Disorder
Sod1-related Disorder
Solar Lentigines (non-facial)
Soluble Urokinase Plasminogen Activator Receptor Levels
Sos1-related Disorder
Spinocerebellar Ataxia Type 42
Spondylolisthesis, Congenital (phecode 754.2)
Spontaneous Preterm Birth with Premature Rupture of Membranes
Sptan1-related Disorder
Subclinical Hypothyroidism in Pregnancy
Succinylcarnitine Levels
Suicide Attempts in Major Depressive Disorder
Suicide Attempts in Major Depressive Disorder or Bipolar Disorder or Schizophrenia
Suicide Attempts in Schizophrenia
Switch to Non-stimulant Treatment in Adhd
Tanner 2 to Tanner 4 Pubertal Stage Transition (joint Longitudinal Bmi and Survival Model)
Tgfbr2 Protein Levels
Thoc6-related Developmental Delay-microcephaly-facial Dysmorphism Syndrome
Thrombocytopenia 13
Thyrotoxic Hypokalemic Periodic Paralysis and Graves Disease
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