Health Conditions
535 conditions with known genetic associations in our database.
All(535)
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)
Blue Vs. Green Eyes
Early Onset and Severe Retinal Dystrophy with Neurological Impairment and Facial Dysmorphia
Early-onset Progressive Neurodegeneration-blindness-ataxia-spasticity Syndrome
Myopia 2
Myopia 23
Myopia 24
Myopia 28
Neurodevelopmental Disorder with Eye Movement Abnormalities and Ataxia
North Carolina Macular Dystrophy
Optic Atrophy 13 with Retinal and Foveal Abnormalities
Progressive Retinal Dystrophy Due to Retinol Transport Defect
Prolonged Electroretinal Response Suppression 2
Response to Ranibizumab in Age-related Macular Degeneration (exudative)
Retinal Detachments and Defects (phecode 361)
Retinal Dystrophy and Microvillus Inclusion Disease
Retinal Hemorrhage/ischemia (phecode 362.8)
Retinal Pigment Epithelial Atrophy
Rhegmatogenous Retinal Detachment
Adult-onset Night Blindness
Age-related Macular Degeneration (extreme Sampling)
Age-related Macular Degeneration (smoking Status Interaction)
Amd or Cataract or Glaucoma (pleiotropy)
Axenfeld-rieger Anomaly with Partially Absent Eye Muscles
Blindness and Low Vision (phecode 367.9)
Cataract or Glaucoma (pleiotropy)
Disorders of Refraction and Accommodation; Blindness and Low Vision (phecode 367)
Eye Color (hue)
Eye Conditions (confirmatory Factor Analysis Factor 25)
Eye Infection, Viral (phecode 369.2)
Fetal Akinesia-cerebral and Retinal Hemorrhage Syndrome
Geographic Atrophy Lesion Growth Rate in Age-related Macular Degeneration
High Myopia-sensorineural Deafness Syndrome
Hypotrichosis with Juvenile Macular Dystrophy
Inflammation of the Eye (phecode 371)
Laterality in Neovascular Age-related Macular Degeneration
Macular Dystrophy with Cone Dysfunction
Macular Dystrophy with or Without Cone Dysfunction
Myopia 21
Other Disorders of Eyelids (phecode 374)
Retinal Arteriolar Width
Retinal Detachment with Retinal Defect (phecode 361.1)
Retinal Dystrophy with Leukodystrophy
Retinal Edema (phecode 362.9)
Retinoschisis and Retinal Cysts (phecode 361.2)
Structural Eye Disease
Abnormal Macular Morphology
Abnormal Retinal Morphology
Age-related Macular Degeneration (snp X Mitochondrial A4917g Interaction)
Age-related Macular Degeneration (snp X Mitochondrial G12771a Interaction)
Autosomal Dominant Rhegmatogenous Retinal Detachment
Blindness, All Causes
Central Retinal Arteriolar Equivalent
Cerebroretinal Microangiopathy with Calcifications and Cysts 2
Chorioretinal Coloboma
Chorioretinal Inflammations, Scars, and Other Disorders of Choroid (phecode 363)
Congenital Blindness
Congenital Muscular Alpha-dystroglycanopathy with Brain and Eye Anomalies
Congenital Stationary Night Blindness 1h
Cystoid Macular Degeneration of Retina (phecode 362.23)
Diabetic Macular Edema
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