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)
Metabolite Peak Levels (qi10664)
Metabolite Peak Levels (qi13749)
Metabolite Peak Levels (qi2815)
Metabolite Peak Levels (qi68)
Metabolite Peak Levels (qi7389)
Metabolite Peak Levels (qi7549)
Metabolite Peak Levels (qi8556)
Metap1d/tst Protein Level Ratio
Metap2/pfkfb2 Protein Level Ratio
Metap2/rilp Protein Level Ratio
Metastatic Melanoma
Methemoglobinemia Type 4
Methionine Adenosyltransferase 2 Subunit Beta Levels
Methionine Sulfoxide Levels
Methotrexate-induced Interstitial Lung Disease in Rheumatoid Arthritis
Methylmalonate (mma) Levels
Methylmalonic Acidemia Due to Transcobalamin Receptor Defect
Methylsuccinate Levels in Elite Athletes
Methyltransferase-like Protein 24 Levels
Metopic Nonsyndromic Craniosynostosis
Mfap5-related Disorder
Mgll/mpig6b Protein Level Ratio
Mgll/shmt1 Protein Level Ratio
Mgll/vta1 Protein Level Ratio
Mgmt Methylation in Smokers
Mhc Class I Deficiency 2
Microalbuminuria in Diabetes
Microcephaly 21
Microcephaly 24
Microcephaly-congenital Cataract-psoriasiform Dermatitis Syndrome
Microcolon
Microcornea
Microfibril-associated Glycoprotein 4 Levels
Mid1-related Disorder
Middle Temporal Gyrus Volume (6 Month Visit)(adjusted For Apoe E4 Dosage)
Midgestational Cytokine/chemokine Levels (maternal Genetic Effect)
Midgestational Total 25-hydroxyvitamin D Levels (fetal Genetic Effect)
Midgestational Total 25-hydroxyvitamin D Levels (maternal Genetic Effect)
Mif/pebp1 Protein Level Ratio
Mif/s100a4 Protein Level Ratio
Mif/stip1 Protein Level Ratio
Migraine or Type 1 Diabetes
Migraine Without Aura (mtag)
Migraine Without Aura And/or Systolic Blood Pressure
Mineral Deficiency Nec (phecode 262)
Mini-mental State Examination / Folstein Test (12 Month Visit)
Mirror Movements 2
Mirror Movements 4
Mitochondrial Cardiomyopathy with or Without Skeletal Myopathy
Mitochondrial Complex Iii Deficiency
Mitochondrial Complex Iii Deficiency Nuclear Type 3
Mitochondrial Dna Heteroplasmy (chrm:16179:ca:c Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:16179:caa:c Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:567:a:acccccc Case-only Heteroplasmy)
Mitochondrial Ubiquitin Ligase Activator of Nfkb 1 Levels
Mitogen-activated Protein Kinase Kinase Kinase Kinase 1 Levels
Mitotic Checkpoint Serine/threonine-protein Kinase Bub1 Levels
Mitral Regurgitation
Mitral Valve Stenosis and Aortic Valve Stenosis (phecode 394.1)
Mkrn3-related Disorder
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