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)
Kiaa0586-related Disorder
Kmt2c-related Disorder
Kmt2c-related Ndd
Koebner Type
Lamc2-related Disorder
Lcn15 Protein Levels
Left Ventricular End Diastolic Mass End Diastolic Volume Ratio
Left Ventricular Wall Thickness (maximal)
Leg Fat Ratio or Breast Cancer (pleiotropy)
Lentiform Nucleus Volume
Lethal Congenital Contracture Syndrome 7
Leukocyte Immunoglobulin-like Receptor Subfamily B Member 2 Levels
Leukoencephalopathy with Vanishing White Matter 2
Liddle Syndrome 3
Lonp1-related Disorder
Low Affinity Immunoglobulin Epsilon Fc Receptor Levels
Lrp4-related Disorder
Lymphatic Malformation 7
Lymphoproliferative Syndrome 2
Lysophosphatidylcholine Levels
Lysophosphatidylethanolamine (16:0) [sn1] Levels
Lysophosphatidylethanolamine (16:0) [sn2] Levels
Macular Puckering of Retina (phecode 362.26)
Malignant Tumor of Testis
Maternal Nondisjunction of Chromosome 21 (mothers Vs Fathers)
Mb Protein Levels
Mcph1-related Disorder
Med18/tbl1x Protein Level Ratio
Median Measurement of Hepatic Fat
Medication Use (antihistamines For Systemic Use)
Medium Chain Acylcarnitines Levels (additive Genetic Model)
Meesmann
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a
Megalocornea
Melanoma-derived Growth Regulatory Protein Levels
Melanomas of Skin (phecode 172.11)
Memory For Intentions Screening Test (mist) Immediate (mist Imd)
Methotrexate-related Central Neurotoxicity in Children Treated For Acute Lymphoblastic Leukemia
Microcephaly 17
Mild Obesity-related Type 2 Diabetes
Mitochondrial Myopathy-lactic Acidosis-deafness Syndrome
Moderate Intellectual Disability
Monocyte Chemoattractant Protein-3 Levels
Monohexosylceramide (d18:1/22:0) Levels
Mpl-related Disorder
Multiple Myeloma (hyperdiploidy)
Mut(0) Type
N-acetylglycine Levels
N-acetylkynurenine (2) Levels
Nad(p)hx Dehydratase Deficiency
Narcolepsy with Cataplexy
Nectin2 Protein Levels
Nectin4 Protein Levels
Nephrotic Syndrome 14
Neurodevelopmental Disorder with Cataracts
Neurodevelopmental Disorder with Cerebellar Atrophy and Motor Dysfunction
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements
Neutrophil Forward Scatter Distribution Width
Nevus Count
Non-proliferative Glomerulonephritis (phecode 580.12)
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →