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)
Free Cholesterol to Total Lipids Ratio in Very Large Hdl
134 variants Metabolic
Juvenile Nephropathic Cystinosis
134 variants Renal
Low Myopia Vs Hyperopia
134 variants Ophthalmic
Mitochondrial Dna Copy Number (raw)
134 variants Other
Neurodegeneration with Brain Iron Accumulation 5
134 variants Other
Total Lipid Levels in Lipoprotein Particles
134 variants Metabolic
Ullrich Congenital Muscular Dystrophy 1a
134 variants Other
Apc-related Disorder
133 variants Other
Free Cholesterol to Total Lipids in Large Hdl Percentage
133 variants Metabolic
Heimler Syndrome 2
133 variants Other
Offspring Birth Weight
133 variants Other
Short-rib Thoracic Dysplasia 14 with Polydactyly
133 variants Other
Sphingomyelin(37:1)_[m+h]1+ Levels
133 variants Other
Takayasu Arteritis
133 variants Other
Adiponectin Levels
132 variants Other
Brain Shape (segment 1)
132 variants Other
Cerebrooculofacioskeletal Syndrome 2
132 variants Other
Charcot-marie-tooth Disease X-linked Dominant 1
132 variants Other
Concentration of Medium Ldl Particles
132 variants Other
Eye Color
132 variants Ophthalmic
Familial Adenomatous Polyposis 3
132 variants Other
Gut Microbial Network Clusters (pink (at 1 Year) X Homesmokers Interaction
132 variants Other
Hereditary Fructosuria
132 variants Other
Long Sleep Duration (>=10 Hours)
132 variants Other
Lymphocyte (absolute Count, Maximum, Inv-norm Transformed)
132 variants Other
Maturity-onset Diabetes of the Young Type 1
132 variants Metabolic
Maturity-onset Diabetes of the Young Type 3
132 variants Metabolic
Mismatch Repair Cancer Syndrome 2
132 variants Cancer
Mitochondrial Dna Depletion Syndrome
132 variants Other
Nephronophthisis 15
132 variants Renal
Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures
132 variants Other
Phospholipids in Very Small Vldl
132 variants Metabolic
Progressive Familial Intrahepatic
132 variants Gastrointestinal
Serum Metabolite Levels (cms)
132 variants Other
Severe Congenital
132 variants Other
Trichorhinophalangeal Dysplasia Type I
132 variants Other
X-linked Severe Combined Immunodeficiency
132 variants Other
Acute
131 variants Other
Autoimmune Thyroid Disease
131 variants Autoimmune
Blue/nonblue Eyes
131 variants Ophthalmic
Cholesteryl Esters to Total Lipids Ratio in Medium Hdl
131 variants Metabolic
Colonoscopy-negative Controls Vs Population Controls
131 variants Other
Crebbp-related Disorder
131 variants Other
Dominant Form
131 variants Other
Eosinophil (absolute Count, Minimum, Inv-norm Transformed)
131 variants Other
Facial Dysmorphism-immunodeficiency-livedo-short Stature Syndrome
131 variants Other
Fanconi Anemia Complementation Group D1
131 variants Hematologic
Free Cholesterol to Total Lipids in Small Hdl Percentage
131 variants Metabolic
Infantile-onset Ascending Hereditary Spastic Paralysis
131 variants Other
Mean Corpuscular Hemoglobin Concentration (mchc, Minimum, Inv-norm Transformed)
131 variants Hematologic
Mpi-congenital Disorder of Glycosylation
131 variants Other
Nephronophthisis 4
131 variants Renal
Orofaciodigital Syndrome I
131 variants Other
Osteogenesis Imperfecta with Normal Sclerae
131 variants Other
Protein Quantitative Trait Loci
131 variants Other
Retinal Disorder
131 variants Ophthalmic
Skin/hair/eye Pigmentation 1
131 variants Dermatologic
Sphingomyelin(44:9)_[m+h]1- Levels
131 variants Other
Systolic Blood Pressure (standard Gwa)
131 variants Cardiovascular
Trans Fatty Acid Levels
131 variants Other
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