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)
3-hydroxy-2-ethylpropionate Levels
4-guanidinobutanoate Levels
4-hydroxychlorothalonil Levels in Elite Athletes
4-hydroxyglutamate Levels in Elite Athletes
4p Partial Monosomy Syndrome
5alpha-androstan-3alpha,17alpha-diol Monosulfate Levels
5alpha-androstan-3alpha,17beta-diol Monosulfate (1) Levels in Elite Athletes
5alpha-androstan-3beta,17alpha-diol Disulfate Levels in Elite Athletes
Abca7-related Disorder
Abhd12-related Disorder
Abnormal Glucose (phecode 250.4)
Abnormal Posture (phecode 781.2)
Abo Blood Group System
Acrbp Protein Levels
Acsf3-related Disorder
Actb-related Bafopathy
Actg1-related Disorder
Acy1 Protein Levels
Ada2-related Disorder
Adamantinous Craniopharyngioma
Adiposity
Adipoylcarnitine (c6-dc) Levels
Adipsin Levels in Overweight Individuals
Adrenomedullin Levels
Adult Onset Neurodegenerative Disorder
Adult-onset Autosomal Dominant Demyelinating Leukodystrophy
Adverse Response to Chemotherapy (neutropenia/leucopenia) (paclitaxel)
Afamin Levels
Agammaglobulinemia 10
Age-related Cognitive Decline (executive Function) (slope of Z-scores)
Aging (time to Event)
Agpat2-related Disorder
Ahsp/hmbs Protein Level Ratio
Al Gazali Type
Al-raqad Syndrome
Alcohol Consumption in Current Drinkers
Alcoholism (heaviness of Drinking)
Aldosterone-producing Adenoma with Seizures and Neurological Abnormalities
Alg1-related Disorder
Alkenylphosphatidylcholine (p-16:0/16:0) Levels
Alkenylphosphatidylcholine (p-17:0/20:4) (a) Levels
Alkenylphosphatidylcholine (p-18:0/20:4) Levels
Alkenylphosphatidylethanolamine (p-16:0/18:2) Levels
Alkenylphosphatidylethanolamine (p-20:1/20:4) Levels
Alpha Angle
Alpha-1-antichymotrypsin Complex Levels
Alpha-2-macroglobulin Levels
Alpha-amylase 2b Levels
Amelogenesis Imperfecta Type 1h
Amot Protein Levels
Ampd1-related Disorder
Amygdala Volume Change Rate X Age Interaction (2df)
Amyotrophic Lateral Sclerosis 27
Analbuminemia
And Ambiguous Genitalia Syndrome
And Arthropathy
And Brittle Hair Syndrome
And Limb Defects
And Myelofibrosis
And Neurodegeneration Syndrome
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