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)
Mn1 C-terminal Truncation (mctt) Syndrome
Monohexosylceramide (d16:1/20:0) Levels
Moyamoya Disease with Early-onset Achalasia
Mpv17-related Disorder
Mpz-related Disorder
Mthfr-related Disorder
Muggenthaler-chowdhury-chioza Syndrome
Multiple Metachronous Adenoma
Multiple Myeloma and Monoclonal Gammopathy
Musculoskeletal Symptoms Referable to Limbs (phecode 771)
Mybpc1 Protein Levels
Myeloperoxidase-dna Complexes
Myocardial Fractal Dimension (slice 4)
Myocardial Fractal Dimension (slice 5)
Myocardial Infarction (early Onset)
Myofibrillar Myopathy 8
N-acetyl-2-aminooctanoate (x-12511) Levels
N-acetyl-aspartyl-glutamate (naag) Levels
N-acetylserine Levels
N-methylpipecolate Levels in Elite Athletes
N2-acetyl,n6,n6-dimethyllysine Levels (advanced Age)
N2-acetyl,n6,n6-dimethyllysine Levels (elderly Offspring)
N2-acetyllysine Levels in Elite Athletes
N4-acetylcytidine Levels
N6-methyllysine Levels (advanced Age)
N6-methyllysine Levels (elderly Offspring)
N6,n6-dimethyllysine Levels
N6,n6-dimethyllysine Levels (advanced Age)
N6,n6-dimethyllysine Levels (elderly Offspring)
Nagk Protein Levels
Naive T-cell Telomere Length
Natural Cytotoxicity Triggering Receptor 3 Levels
Ndufv1-related Disorder
Neonatal Circulating Complement Component 3 (c3) Protein Concentration
Neonatal Encephalopathy
Nephrotic Range Proteinuria
Nervonoylcarnitine (c24:1) Levels
Netrin-1 Levels
Neural Cell Adhesion Molecule 1, 120 Kda Isoform Levels
Neurocognitive Impairment in Hiv-1 Infection (dichotomous)
Neurodevelopmental Disorder with Gait Disturbance
Neurodevelopmental Disorder with Hypotonia and Cerebellar Atrophy
Neurodevelopmental Disorder with Hypotonia and Characteristic Brain Abnormalities
Neurodevelopmental Disorder with or Without Variable Movement or Behavioral Abnormalities
Neurodevelopmental Disorder with Visual Defects and Brain Anomalies
Neurogenic Locus Notch Homolog Protein 1 Levels
Neurooculocardiogenitourinary Syndrome
Neutrophil Collagenase Levels
Non-ischemic Heart Failure with Reduced Ejection Fraction
Non-oily Fish Consumption
Non-oral Lichen Planus
Non-syndromic X-linked Intellectual Disability
Nonsyndromic Cleft Lip Palate
Ntprobnp Protein Levels
Nuclear Type 26
Nucleus Accumbens Volume Change Rate X Age Interaction (2df)
Nystagmus 6
Obesity Class Ii and Attention Deficit Hyperactivity Disorder or Anorexia Nervosa or Major Depressive Disorder or Obsesive-compulsive Disorder or Schizophrenia
Obstructive Sleep Apnea (phecode 327.32)
Obstructive Sleep Apnea Trait (minimum Oxyhemoglobin Saturation Across Sleep Episode)
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