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)
Hereditary Spastic Paraplegia 3a
Megf10-related Myopathy
Morning Vs. Evening Chronotype
Oculocutaneous Albinism
Saethre-chotzen Syndrome
Xanthinuria Type Ii
Acromicric Dysplasia
Adgrv1-related Disorder
Amyotrophic Lateral Sclerosis (sporadic)
Asphyxiating Thoracic Dystrophy 4
Endometriosis (mtag)
Fev1 X Serum 25-hydroxyvitamin D Interaction in Ever Smokers (2df Test)
Itch Intensity From Mosquito Bite
Mucopolysaccharidosis Type 7
Pla2g6-associated Neurodegeneration
Pregnancy Loss in Nulliparas
Rosacea Symptom Severity
White Matter Hyperintensity Volume
White Matter Microstructure (mode of Anisotropy)
Age-related Hearing Impairment (snp X Snp Interaction)
Aspartylglucosaminuria
Autosomal Recessive 53
Basophil (fraction, Minimum, Inv-norm Transformed)
Biotin-responsive Basal Ganglia Disease
Bitter Alcoholic Beverage Consumption
Cd109 Protein Levels
Charcot-marie-tooth Disease Type 4a
Clec4c Protein Levels
Col7a1-related Disorder
Deficiency of Aromatic-l-amino-acid Decarboxylase
Dystonia 5
Glucocorticoid-remediable Aldosteronism
Hyperphosphatasia with Intellectual Disability Syndrome 2
Intellectual Disability-microcephaly-strabismus-behavioral Abnormalities Syndrome
Potassium-aggravated Myotonia
Severe Combined Immunodeficiency Due to Card11 Deficiency
Triglyceride Levels in Very Large Vldl
Ahdc1-related Intellectual Disability - Obstructive Sleep Apnea - Mild Dysmorphism Syndrome
Autosomal Dominant Optic Atrophy Classic Form
Body Fat Distribution (trunk Fat Ratio)
Ceroid Lipofuscinosis
Dextro-looped Transposition of the Great Arteries
Hydrocephalus
Hypertrophic Cardiomyopathy 9
Pick Disease
Psca Protein Levels
Singleton-merten Syndrome 1
Syne1-related Disorder
Tmprss5 Protein Levels
And Dysmorphic Facies
And Impaired Language
Cannabis Use Disorder (mtag)
Cog5-congenital Disorder of Glycosylation
Cyclical Neutropenia
Factor V Deficiency
Generalized Juvenile Polyposis/juvenile Polyposis Coli
Glucose Levels (ukb Data Field 30740)
Joubert Syndrome 1
Luscan-lumish Syndrome
Lysosomal Acid Lipase Deficiency
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