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)
Mhc Class I Deficiency 1
Mhc Class Ii Deficiency 5
Mib1-related Disorder
Micb_mica/tek Protein Level Ratio
Micos Complex Subunit Mic10 Levels (minos1.7956.11.3)
Microcephaly 11
Microcephaly 23
Microcephaly 30
Microcephaly and Chorioretinopathy with or Without Intellectual Disability
Microdontia
Microtubule-associated Protein Tau Levels
Mid-point of the Five Least Active Hours of the Day
Middle Temporal Gyrus Volume (12 Month Visit)
Middle Temporal Gyrus Volume (24 Month Visit)
Middle Temporal Gyrus Volume (baseline)(adjusted For Apoe E4 Dosage)
Midgestational Circulating Levels of Organochlorine Pesticides
Midgestational Total 25-hydroxyvitamin D Levels (antenatal Blood)
Midkine Levels
Midline Nonsyndromic Craniosynostosis
Midregional Pro Atrial Natriuretic Peptide Levels
Mif/serpinb1 Protein Level Ratio
Mild Canavan Disease
Mild Form
Mild Hyperphenylalaninemia
Mild to Moderate Ndd
Milk Allergy (maternal Genetic Effects)
Milk Allergy (parent-of-origin Effect)
Milk Type: Skimmed, Semi-skimmed or Full Cream (ukb Data Field 1418)
Mimecan Levels
Mineralocorticoid Receptor Levels
Mini-mental State Examination / Folstein Test (12 Month Visit)(adjusted For Apoe E4 Dosage)
Mini-mental State Examination / Folstein Test (6 Month Visit)(adjusted For Apoe E4 Dosage)
Mini-mental State Examination / Folstein Test (baseline)(adjusted For Apoe E4 Dosage)
Minimum Ankle–brachial Index
Mip-related Disorder
Mitd1/snx9 Protein Level Ratio
Mitochondrial Complex 1 Deficiency
Mitochondrial Complex Iii Deficiency Nuclear Type 6
Mitochondrial Complex Iii Deficiency Nuclear Type 7
Mitochondrial Cytochrome C Oxidase Deficiency
Mitochondrial Dna Depletion Syndrome 17
Mitochondrial Dna Depletion Syndrome 18
Mitochondrial Dna Depletion Syndrome 8b (mngie Type)
Mitochondrial Dna Heteroplasmy (chrm:16182:a:ac Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:16182:a:c Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:16183:a:ac Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:16183:a:acccc Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:955:a:ac Case-only Heteroplasmy)
Mitochondrial Dna-associated Leigh Syndrome and Narp
Mitochondrial Import Inner Membrane Translocase Subunit Tim14 Levels
Mitochondrial Import Inner Membrane Translocase Subunit Tim21 Levels
Mitochondrial Myopathy
Mitochondrial Ubiquitin Ligase Activator of Nfkb 1 Levels (mul1.9315.16.3)
Mitogen-activated Protein Kinase 1 Levels
Mitogen-activated Protein Kinase 13 Levels (mapk13.5006.71.1)
Mitogen-activated Protein Kinase 14 Levels
Mixed Cryoglobulinemia Vasculitis in Chronic Hepatitis C Infection
Miyoshi Myopathy
Mki67-related Disorder
Mmp-1 Levels
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