Health Conditions

43,676 conditions with known genetic associations in our database.

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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)
Nags-related Disorder
3 variants Other
Naive-mature B Cell %b Cell
3 variants Other
Nanophthalmos 4
3 variants Other
Narcolepsy (age of Onset)
3 variants Other
Nat2-related Disorder
3 variants Other
Natriuretic Peptide Levels
3 variants Other
Natural Killer %cd3- Lymphocyte
3 variants Other
Natural Killer %lymphocyte
3 variants Other
Natural Killer T %t Cell
3 variants Other
Nbl1/nectin4 Protein Level Ratio
3 variants Other
Nbl1/tgfbr2 Protein Level Ratio
3 variants Other
Nbn/nmnat1 Protein Level Ratio
3 variants Other
Ncf2/padi4 Protein Level Ratio
3 variants Other
Nde1-related Disorder
3 variants Other
Nde1-related Microhydranencephaly
3 variants Other
Ndufs3-related Disorder
3 variants Other
Ndufs4-related Disorder
3 variants Other
Ndufs8-related Disorder
3 variants Other
Nectin2/tnfrsf14 Protein Level Ratio
3 variants Other
Nedd8-conjugating Enzyme Ube2f Levels
3 variants Other
Nemaline Myopathy 3
3 variants Other
Neonatal (c3dc+c4-oh) to Decanoylcarnitine Ratio (maternal Genotype Effect)
3 variants Other
Neonatal Adipoylcarnitine (c6dc) Levels (maternal Genotype Effect)
3 variants Other
Neonatal Cytokine/chemokine Levels (maternal Genetic Effect)
3 variants Other
Neonatal Hexanoylcarnitine (c6) Levels (maternal Genotype Effect)
3 variants Other
Neonatal Jaundice (maternal Effect)
3 variants Other
Neonatal Octanoylcarnitine (c8) Levels (maternal Genotype Effect)
3 variants Other
Neonatal Onset
3 variants Other
Nerve Root Lesions (phecode 353.2)
3 variants Other
Netrin Receptor Unc5b (analyte X7776.20) Levels
3 variants Other
Netrin Receptor Unc5b Levels
3 variants Other
Netrin Receptor Unc5d Levels
3 variants Other
Netrin-4 Levels
3 variants Other
Neu1-related Disorder
3 variants Other
Neural Cell Adhesion Molecule 1, 120 Kda Isoform Levels (ncam1.4498.62.2)
3 variants Other
Neural Cell Adhesion Molecule 2 Levels (ncam2.6507.16.3)
3 variants Other
Neuralized-like Protein 4 Levels
3 variants Other
Neuregulin-4 Levels
3 variants Other
Neurexophilin-1 Levels (nxph1.4562.1.2)
3 variants Other
Neuritic Plaques or Cerebral Amyloid Angiopathy (pleiotropy)
3 variants Other
Neuritic Plaques or Neurofibrillary Tangles or Cerebral Amyloid Angiopathy (pleiotropy)
3 variants Other
Neurocan Core Protein Levels
3 variants Other
Neurodegeneration with Brain Iron Accumulation 7
3 variants Other
Neurodevelopmental Disorder with Cerebellar Hypoplasia and Spasticity
3 variants Other
Neurodevelopmental Disorder with Dysmorphic Facies and Ischiopubic Hypoplasia
3 variants Other
Neurodevelopmental Disorder with Dystonia and Seizures
3 variants Other
Neurodevelopmental Disorder with Microcephaly and Speech Delay
3 variants Other
Neurodevelopmental Disorder with Short Stature
3 variants Other
Neurodevelopmental Disorder with Spastic Quadriplegia and Brain Abnormalities with or Without Seizures
3 variants Other
Neurodevelopmental Disorder with Spasticity and Poor Growth
3 variants Other
Neurodevelopmental Disorder with Speech Impairment and with or Without Seizures
3 variants Other
Neurofascin Levels (nfasc.7179.69.3)
3 variants Other
Neurofilament Light Polypeptide Levels
3 variants Other
Neuroligin-4, X-linked Levels
3 variants Other
Neurological Involvement in Behcet's Disease
3 variants Other
Neuromedin-b Levels
3 variants Other
Neuromodulin Levels
3 variants Other
Neuromyelitis Optica
3 variants Other
Neuronal Pentraxin Receptor Levels
3 variants Other
Neuronal Pentraxin-1 Levels
3 variants Other
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