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)
Manf/pmvk Protein Level Ratio
Map Kinase-activated Protein Kinase 3 Levels
Mastocytosis (kit D816v Positive)
Matrix Metalloproteinase-10 Levels
Matrix Metalloproteinase-12 Levels
Mbd4-related Disorder
Mccune-albright Syndrome
Medium Hdl Particle Concentration
Medium Ldl Particle Concentration
Medulloblastoma Shh Activated and Tp53 Mutant
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Syndrome 3
Men2 Phenotype: Unclassified
Menorrhagia
Mental Composite Score
Mesd/nck2 Protein Level Ratio
Metabolite Levels (3-aminoisobutyrate; __aminoisobutyrate)
Metabolite Levels (carnitine)
Metabolite Levels (n-acetylcarnosine)
Metabolite Levels (n-acetyltryptophan)
Metabolite Risk Score For Predicting Weight Gain
Metabolonic Lactone Sulfate Levels (advanced Age)
Metabolonic Lactone Sulfate Levels (elderly Offspring)
Metap1d Protein Levels
Methyl Glucopyranoside (alpha + Beta) Levels in Elite Athletes
Mgll/ptpn6 Protein Level Ratio
Microcephaly 26
Microcephaly and Chorioretinopathy 2
Microfibrillar-associated Protein 2 Levels
Middle Childhood and Early Adolescence Aggressive Behavior
Middle Temporal Gyrus Volume
Middle Temporal Thickness
Mitochondrial Complex Iii Deficiency Nuclear Type 8
Mitochondrial Encephalomyopathy
Mitogen-activated Protein Kinase 8 Levels
Mitral Valve Prolapse After Mitral Valve Surgery
Mmaa-related Disorder
Moderate or Severe Diarrhoea in Darapladib-treated Cardiovascular Disease (time to Event)
Monobrow Thickness
Monocarboxylate Transporter 1 Deficiency
Monocyte Percentage of White Cells Variance
Monohexosylceramide (d18:2/20:0) Levels
Motor Coordination
Motor Premotor Thickness
Moyamoya Disease 5
Mpo-related Disorder
Mtdh Protein Levels
Mtif3 Protein Levels
Multiple Congenital Anomalies-neurodevelopmental Syndrome
Multiple Mitochondrial Dysfunctions Syndrome 9b
Multiple Myeloma (phecode 204.4)
Myelin Protein P0 Levels
Myeloid Clonal Hematopoiesis
Myh9 Protein Levels
Myo1e-related Disorder
Myoclonic Dystonia 26
Myofibrillar Myopathy
Myofibrillar Myopathy 7
Myotonia
Myristoylcarnitine Levels
N-acetylalanine Levels
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →