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)
Kallikrein-12 Levels
13 variants Other
Kallistatin Levels
13 variants Pharmacogenomic
Kcna3-associated Developmental and Epileptic Encephalopathy
13 variants Other
Killer Cell Immunoglobulin-like Receptor 2dl5a Levels (kir2dl5a.8000.17.3)
13 variants Other
Kras-related Disorder
13 variants Other
Krt5-related Disorder
13 variants Other
Lactosyl-n-palmitoyl-sphingosine Levels
13 variants Other
Lamb3-related Disorder
13 variants Other
Lap Tgf Beta1 Levels
13 variants Other
Lateral Nucleus Volume
13 variants Other
Lateral Orbital Frontal Cortex Volume
13 variants Other
Ldl-cholesterol Level in Antipsychotic-treated Schizophrenia (4-week)
13 variants Neurological
Leber Congenital Amaurosis 16
13 variants Other
Left Atrial Minimum Volume Bsa Indexed
13 variants Other
Lifespan
13 variants Other
Lifetime Major Depressive Disorder (softimpute)
13 variants Other
Liver Proton Density Fat Fraction
13 variants Gastrointestinal
Liver Stiffness Changes At Sustained Virological Response Following Antiviral Therapy in Hcv Infection
13 variants Gastrointestinal
Liver Volume
13 variants Gastrointestinal
Low Susceptibility to Hepatitis C Infection
13 variants Other
Lower Motor Neuron Syndrome with Late-adult Onset
13 variants Other
Lpin2-related Disorder
13 variants Other
Lysophosphatidylethanolamine (18:0) [sn1] Levels
13 variants Other
Lysophosphatidylethanolamine (18:0) [sn2] Levels
13 variants Other
Lysophosphatidylethanolamine_16:0_[m-h]1- Levels
13 variants Other
Macular Degeneration (senile) of Retina Nos (phecode 362.29)
13 variants Ophthalmic
Major Depressive Disorder or Stroke (pleiotropy)
13 variants Cardiovascular
Malunion and Nonunion of Fracture (phecode 733.8)
13 variants Musculoskeletal
Maternal Nondisjunction of Chromosome 21 (mii Error Vs Fathers)
13 variants Other
Maximum Stenosis
13 variants Other
Mean Corpuscular Hemoglobin Variance
13 variants Hematologic
Mean Corpuscular Volume Variance
13 variants Other
Megf10-related Disorder
13 variants Other
Mesothelioma
13 variants Other
Metabolite Levels (5-hiaa)
13 variants Other
Metabolite Levels (hva)
13 variants Other
Metaphyseal Anadysplasia 2
13 variants Other
Methylmalonate Semialdehyde Dehydrogenase Deficiency
13 variants Other
Mfap5 Protein Levels
13 variants Other
Mmp7 Protein Levels
13 variants Other
Mocs1-related Disorder
13 variants Other
Moderate to Vigorous Physical Activity Levels
13 variants Other
Moderate-to-vigorous Intensity Physical Activity During Leisure Time
13 variants Other
Monocyte Side Fluorescence Distribution Width
13 variants Other
Monohexosylceramide (d16:1/22:0) Levels
13 variants Other
Monohexosylceramide (d18:2/24:0) Levels
13 variants Other
Mri1 Protein Levels
13 variants Other
Mstn Protein Levels
13 variants Other
Mullegama-klein-martinez Syndrome
13 variants Other
Multiple Synostoses Syndrome 2
13 variants Other
Musculocontractural Type 1
13 variants Other
Myopia 6
13 variants Ophthalmic
N-acetyl-isoputreanine (x-12688) Levels
13 variants Other
Narcolepsy
13 variants Other
Nasal Polyposis (mtag)
13 variants Other
Nephroblastoma
13 variants Renal
Neuroblastoma (pediatric)
13 variants Other
Neurodevelopmental Disorder with Dysmorphic Facies
13 variants Other
Neurodevelopmental Disorder with Facial Dysmorphism
13 variants Other
Neurodevelopmental Disorder with Progressive Microcephaly
13 variants Other
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