Health Conditions
43,676 conditions with known genetic associations in our database.
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)
Myh9-related Disorder
Perinatal Lethal
Regional Enteritis
X-linked 102
Abdominal Fat Cell Number
Abnormality of the Nervous System
Acyl-coa Dehydrogenase 9 Deficiency
Essential Thrombocythemia
Mild
Mitochondrial Dna Depletion Syndrome 13
Omega-3 Fatty Acids Levels
Omega-6 Fatty Acid Percentage of Total Fatty Acids
Pyropoikilocytosis
Severe Feeding Difficulties-failure to Thrive-microcephaly Due to Asxl3 Deficiency Syndrome
Triglyceride (minimum, Inv-norm Transformed)
Ataxia-telangiectasia-like Disorder 1
Autosomal Recessive 4
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2e
Blepharophimosis - Intellectual Disability Syndrome
Mitochondrial Dna Copy Number (raw)
Neurodegeneration with Brain Iron Accumulation 5
Ullrich Congenital Muscular Dystrophy 1a
Apc-related Disorder
Heimler Syndrome 2
Offspring Birth Weight
Short-rib Thoracic Dysplasia 14 with Polydactyly
Sphingomyelin(37:1)_[m+h]1+ Levels
Takayasu Arteritis
Adiponectin Levels
Brain Shape (segment 1)
Cerebrooculofacioskeletal Syndrome 2
Charcot-marie-tooth Disease X-linked Dominant 1
Concentration of Medium Ldl Particles
Familial Adenomatous Polyposis 3
Gut Microbial Network Clusters (pink (at 1 Year) X Homesmokers Interaction
Hereditary Fructosuria
Long Sleep Duration (>=10 Hours)
Lymphocyte (absolute Count, Maximum, Inv-norm Transformed)
Mitochondrial Dna Depletion Syndrome
Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures
Serum Metabolite Levels (cms)
Severe Congenital
Trichorhinophalangeal Dysplasia Type I
X-linked Severe Combined Immunodeficiency
Acute
Colonoscopy-negative Controls Vs Population Controls
Crebbp-related Disorder
Dominant Form
Eosinophil (absolute Count, Minimum, Inv-norm Transformed)
Facial Dysmorphism-immunodeficiency-livedo-short Stature Syndrome
Infantile-onset Ascending Hereditary Spastic Paralysis
Mpi-congenital Disorder of Glycosylation
Orofaciodigital Syndrome I
Osteogenesis Imperfecta with Normal Sclerae
Protein Quantitative Trait Loci
Sphingomyelin(44:9)_[m+h]1- Levels
Trans Fatty Acid Levels
Type 9
Verbal Learning
Visceral
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