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)
Mgll/skap2 Protein Level Ratio
2 variants Other
Mhc Class I Deficiency 1
2 variants Other
Mhc Class Ii Deficiency 5
2 variants Other
Mib1-related Disorder
2 variants Other
Micb_mica/tek Protein Level Ratio
2 variants Other
Micos Complex Subunit Mic10 Levels (minos1.7956.11.3)
2 variants Other
Microcephaly 11
2 variants Other
Microcephaly 23
2 variants Other
Microcephaly 30
2 variants Other
Microcephaly and Chorioretinopathy with or Without Intellectual Disability
2 variants Other
Microdontia
2 variants Other
Microscopic Colitis
2 variants Autoimmune
Microtubule-associated Protein Tau Levels
2 variants Other
Mid-point of the Five Least Active Hours of the Day
2 variants Other
Middle Temporal Gyrus Volume (12 Month Visit)
2 variants Other
Middle Temporal Gyrus Volume (24 Month Visit)
2 variants Other
Middle Temporal Gyrus Volume (baseline)(adjusted For Apoe E4 Dosage)
2 variants Other
Midgestational Circulating Levels of Organochlorine Pesticides
2 variants Other
Midgestational Total 25-hydroxyvitamin D Levels (antenatal Blood)
2 variants Other
Midkine Levels
2 variants Other
Midline Nonsyndromic Craniosynostosis
2 variants Other
Midregional Pro Atrial Natriuretic Peptide Levels
2 variants Other
Mif/serpinb1 Protein Level Ratio
2 variants Other
Migraine Headaches
2 variants Neurological
Migraine or Homa-b
2 variants Neurological
Migraine with Aura And/or Diastolic Blood Pressure
2 variants Cardiovascular
Migraine with Aura And/or Pulse Pressure
2 variants Neurological
Migraine with Aura And/or Systolic Blood Pressure
2 variants Cardiovascular
Mild Canavan Disease
2 variants Other
Mild Form
2 variants Other
Mild Hemophilia A
2 variants Hematologic
Mild Hyperphenylalaninemia
2 variants Other
Mild Non-pku Hyperphenylalanemia
2 variants Hematologic
Mild to Moderate Ndd
2 variants Other
Milk Allergy (maternal Genetic Effects)
2 variants Other
Milk Allergy (parent-of-origin Effect)
2 variants Other
Milk Type: Skimmed, Semi-skimmed or Full Cream (ukb Data Field 1418)
2 variants Other
Mimecan Levels
2 variants Other
Mineralocorticoid Receptor Levels
2 variants Other
Mini-mental State Examination / Folstein Test (12 Month Visit)(adjusted For Apoe E4 Dosage)
2 variants Other
Mini-mental State Examination / Folstein Test (6 Month Visit)(adjusted For Apoe E4 Dosage)
2 variants Other
Mini-mental State Examination / Folstein Test (baseline)(adjusted For Apoe E4 Dosage)
2 variants Other
Minimum Ankle–brachial Index
2 variants Other
Mip-related Disorder
2 variants Other
Mitd1/snx9 Protein Level Ratio
2 variants Other
Mitochondrial Complex 1 Deficiency
2 variants Other
Mitochondrial Complex Iii Deficiency Nuclear Type 6
2 variants Other
Mitochondrial Complex Iii Deficiency Nuclear Type 7
2 variants Other
Mitochondrial Cytochrome C Oxidase Deficiency
2 variants Other
Mitochondrial Dna Depletion Syndrome 16 (hepatic Type)
2 variants Gastrointestinal
Mitochondrial Dna Depletion Syndrome 17
2 variants Other
Mitochondrial Dna Depletion Syndrome 18
2 variants Other
Mitochondrial Dna Depletion Syndrome 8b (mngie Type)
2 variants Other
Mitochondrial Dna Heteroplasmy (chrm:16182:a:ac Case-only Heteroplasmy)
2 variants Other
Mitochondrial Dna Heteroplasmy (chrm:16182:a:c Case-only Heteroplasmy)
2 variants Other
Mitochondrial Dna Heteroplasmy (chrm:16183:a:ac Case-only Heteroplasmy)
2 variants Other
Mitochondrial Dna Heteroplasmy (chrm:16183:a:acccc Case-only Heteroplasmy)
2 variants Other
Mitochondrial Dna Heteroplasmy (chrm:955:a:ac Case-only Heteroplasmy)
2 variants Other
Mitochondrial Dna-associated Leigh Syndrome and Narp
2 variants Other
Mitochondrial Import Inner Membrane Translocase Subunit Tim14 Levels
2 variants Other
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