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)
Hypophosphatemic Rickets
Type Vii
Basophil (fraction, Maximum, Inv-norm Transformed)
Blood Cell Traits Latent Factor 14 (red Cell)
Cholesteryl Ester(20:4)_[m+nh4]1+ Levels
Chromosome 2q32-q33 Deletion Syndrome
Cognitive Empathy
Dysarthria
Hemochromatosis Type 3
Hereditary Systemic 1
Neuronal Ceroid Lipofuscinosis 5
With Variable Foci 3
Aspartate Aminotransferase (ast, Minimum, Inv-norm Transformed)
Autosomal Recessive 1
Bardet-biedl Syndrome 12
Cowden Syndrome 3
Depressive Symptoms (mtag)
Leber Congenital Amaurosis 13
Lynch-like Syndrome
Msh6-related Disorder
Odonto-onycho-dermal Dysplasia
Potassium (mean, Inv-norm Transformed)
Pseudohypoaldosteronism
Stickler Syndrome Type 2
Triglyceride Levels in Vldl
Wolman Disease
Alg1-congenital Disorder of Glycosylation
Autosomal Recessive Nonsyndromic Hearing Loss 97
Cone-rod Dystrophy 2
Eichsfeld Type Congenital Muscular Dystrophy
Gm1 Gangliosidosis Type 2
Grn-related Frontotemporal Lobar Degeneration with Tdp43 Inclusions
Leucine Levels
Neurodevelopmental Disorder with Microcephaly
Noonan Syndrome 4
Pura-related Severe Neonatal Hypotonia-seizures-encephalopathy Syndrome
Familial Spontaneous Pneumothorax
Fvc X Serum 25-hydroxyvitamin D Interaction in Never Smokers (2df Test)
Gut Microbial Network Clusters (blueviolet (at 3 Months) X Household Furry Pet Dog (3 Months) Interaction
Mevalonic Aciduria
Thrombophilia Due to Thrombin Defect
Triglyceride Levels in Small Vldl
Von Willebrand Disease Type 1
Bardet-biedl Syndrome 13
Disseminated Superficial Actinic Type
Fraser Syndrome 2
Gm1 Gangliosidosis Type 3
Holoprosencephaly 7
Methylcobalamin Deficiency Type Cblg
Methylmalonic Acidemia
Omega-6 Fatty Acids Levels
Wfs1-related Spectrum Disorders
Alanine Transaminase (alt, Mean, Inv-norm Transformed)
Brittle Cornea Syndrome 1
Lissencephaly Due to Lis1 Mutation
Medication Use (beta Blocking Agents)
Myh7-related Skeletal Myopathy
Myosin Storage Myopathy
Number of Sexual Partners
Porokeratosis 3
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