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)
Myelodysplasia
Myeloproliferative Disorder
Myh8-related Disorder
Myocardial Fractal Dimension (slice 8)
Myoclonus (phecode 333.2)
Myopathy Due to Calsequestrin and Serca1 Protein Overload
Myosin Regulatory Light Chain 2, Atrial Isoform Levels
Myristoyl Dihydrosphingomyelin (d18:0/14:0) Levels in Elite Athletes
N-(2-furoyl)glycine Levels in Elite Athletes
N-acetyl-1-methylhistidine Levels in Elite Athletes
N-acetyl-cadaverine Levels in Elite Athletes
N-acetylalanine Levels in Elite Athletes
N-acetylcitrulline Levels
N-acetylcitrulline Levels in Elite Athletes
N-acetyllactosaminide Beta-1,3-n-acetylglucosaminyltransferase 2 Levels
N-acetylputrescine Levels in Elite Athletes
N-methylpipecolate Levels
N-oleoyltaurine Levels in Elite Athletes
N-stearoyl-sphingosine (d18:1/18:0) Levels
N-trimethyl 5-aminovalerate Levels in Elite Athletes
N1-methyl-2-pyridone-5-carboxamide Levels in Elite Athletes
N1-methyladenosine Levels
N6-carbamoylthreonyladenosine Levels in Elite Athletes
N6-carboxymethyllysine Levels in Elite Athletes
Nagashima Type
Nars2-related Disorder
Nbea-related Disorder
Nbn Protein Levels
Ncf2 Protein Levels
Ncf2-related Disorder
Nck2/vash1 Protein Level Ratio
Ndufs1-related Disorder
Ndufs2-related Disorder
Neonatal Severe
Neuferricin Levels
Neural Cell Adhesion Molecule L1-like Protein Levels
Neuregulin-1, Sensory and Motor Neuron-derived Factor Isoform Levels
Neurocardiofaciodigital Syndrome
Neurocognitive Impairment in Hiv-1 Infection (continuous)
Neurodevelopmental Disorder with Growth Retardation
Neurodevelopmental Disorder with Hypotonia and Autistic Features with or Without Hyperkinetic Movements
Neurodevelopmental Disorder with Hypotonia and Dysmorphic Facies
Neurodevelopmental Disorder with Infantile Epileptic Spasms
Neurodevelopmental Disorder with Neuromuscular and Skeletal Abnormalities
Neurodevelopmental Disorder with Poor Growth and Behavioral Abnormalities
Neurodevelopmental Disorder with Speech Delay and Variable Ocular Anomalies
Neutrophil Count Variance
Neutrophil Immunodeficiency Syndrome
Neutrophil Percentage of White Cells Variance
Nexn-related Disorder
Nicotine Use
Nlrc4-related Disorder
Noelin-3 Levels
Nog-related Disorder
Non-response to Bupropion and Depression
Non-syndromic Oligodontia
Nonspecific Abnormal Findings On Radiological and Other Examination of Biliary Tract (phecode 575.9)
Nonsyndromic Congenital Nail Disorder 1
Noonan Syndrome 12
Nppc Protein Levels
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