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)
Ltbp4-related Disorder
11 variants Other
Lymphocyte Side Scatter Distribution Width
11 variants Other
Lymphoid Leukemia, Chronic (phecode 204.12)
11 variants Cancer
Lymphoid Neoplasms (somatic Mutation Group 1 Phenocluster)
11 variants Cancer
Mackerel Liking
11 variants Other
Macrothrombocytopenia-lymphedema-developmental Delay-facial Dysmorphism-camptodactyly Syndrome
11 variants Other
Major Depressive Disorder or Glomerular Filtration Rate Estimated From Cystatin (mtag)
11 variants Pharmacogenomic
Margaroylcarnitine Levels in Elite Athletes
11 variants Other
Maximum Measurement of Hepatic Fat
11 variants Gastrointestinal
Mccc2-related Disorder
11 variants Other
Mcp2 Levels
11 variants Other
Mean Platelet Volume Variance
11 variants Hematologic
Medium Chain Acylcarnitines Levels (dominant Genetic Model)
11 variants Other
Meester-loeys Syndrome
11 variants Other
Megacystis-microcolon-intestinal Hypoperistalsis Syndrome 5
11 variants Other
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus Syndrome 1
11 variants Other
Mend Syndrome
11 variants Other
Metabolite Levels (5-hiaa/ Mhpg Ratio)
11 variants Other
Mhc Class Ii Deficiency 2
11 variants Other
Microphthalmia with Limb Anomalies
11 variants Other
Microtubule-associated Proteins 1a/1b Light Chain 3a Levels
11 variants Other
Mild Variant
11 variants Other
Minimum Measurement of Hepatic Fat
11 variants Gastrointestinal
Mitochondrial Dna Depletion Syndrome 14 (cardioencephalomyopathic Type)
11 variants Other
Monohexosylceramide (d16:1/24:0) Levels
11 variants Other
Monohexosylceramide (d18:2/22:0) Levels
11 variants Other
Motor Premotor Thickness (unadjusted For Global Measures)
11 variants Other
Motor Progression (time to Event) in Parkinson's Disease
11 variants Neurological
Moyamoya Angiopathy with Developmental Delay
11 variants Other
Mtr-related Disorder
11 variants Other
Multiple Keratinocyte Cancers
11 variants Cancer
Multisystemic Smooth Muscle Dysfunction Syndrome
11 variants Other
Myh2-related Disorder
11 variants Other
Myocardial Fractal Dimension (slice 6)
11 variants Other
Myoepithelial Tumor
11 variants Cancer
Myopathy with Abnormal Lipid Metabolism
11 variants Metabolic
N-acetylleucine Levels
11 variants Other
N-delta-acetylornithine Levels in Elite Athletes
11 variants Other
N-formylmethionine Levels
11 variants Other
Nausea Incidence in Varenicline-treated Smokers
11 variants Other
Neonatal Cytokine/chemokine Levels (fetal Genetic Effect)
11 variants Other
Nephronophthisis 20
11 variants Renal
Neurexophilin-1 Levels
11 variants Other
Neurodevelopmental Disorder with Epilepsy
11 variants Neurological
Neurodevelopmental Disorder with or Without Autistic Features And/or Structural Brain Abnormalities
11 variants Other
Neuroocular Syndrome 1
11 variants Other
Nonrheumatic Aortic Valve Disorders (phecode 395.2)
11 variants Cardiovascular
Nonsyndromic Congenital Nail Disorder 4
11 variants Other
Normophosphatemic Familial Tumoral Calcinosis
11 variants Cancer
Npr2-related Disorder
11 variants Other
Nr2e3-related Disorder
11 variants Other
Nr5a1-related Disorder
11 variants Other
Number of Children (6+ Vs. 0 or 1)
11 variants Other
Odor Identification (cinnamon)
11 variants Other
Oocyte Maturation Defect 14
11 variants Other
Optic Atrophy 10 with or Without Ataxia
11 variants Other
Optn-related Disorder
11 variants Other
Oral Microbiome Beta Diversity (bray-curtis) in Oral Squamous Cell Carcinoma
11 variants Cancer
Osm Protein Levels
11 variants Other
Osteogenesis Imperfecta Type 9
11 variants Other
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