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)
N-acetylarginine Levels in Elite Athletes
N-acetylglucosaminylasparagine Levels
N-acetylglutamine Levels in Elite Athletes
N-acetylmethionine Levels in Elite Athletes
N-acetyltryptophan Levels
N,n,n-trimethyl-5-aminovalerate Levels
N6,n6,n6-trimethyllysine Levels
Nad-dependent Protein Deacylase Sirtuin-5, Mitochondrial Levels
Nbl1 Protein Levels
Nectin1-related Disorder
Neonatal Total 25-hydroxyvitamin D Levels (maternal Genetic Effect)
Netrin Receptor Unc5c Levels
Neural Cell Adhesion Molecule 2 Levels
Neurocognitive Measure (copy Accuracy) in Obsessive-compulsive Disorder
Neurodevelopmental
Neurodevelopmental Disorder with Behavioral Abnormalities
Neurodevelopmental Disorder with Cerebral Atrophy and Variable Facial Dysmorphism
Neurodevelopmental Disorder with Hypotonia and Speech Delay
Neurodevelopmental Disorder with Language Delay and Behavioral Abnormalities
Neurodevelopmental Disorder with Poor Growth
Neurodevelopmental Disorder with Poor Language and Loss of Hand Skills
Neurodevelopmental Disorder with Seizures and Gingival Overgrowth
Neuroticism Group Factors (depression)
Nexmif-related Disorder
Nidogen-1 Levels
Nkx2-1-related Disorder
Non-progressive Neurodevelopmental Disorder with Spasticity and Transient Opisthotonus
Non-receptor Tyrosine-protein Kinase Tyk2 Levels
Non-word Repetition
Nonanoylcarnitine (c9) Levels
Noncompaction Cardiomyopathy
Nonspecific Abnormal Findings On Radiological and Other Examination of Skull and Head (phecode 346.1)
Nonsyndromic Congenital Nail Disorder 8
Nonsyndromic Sensorineural Hearing Loss
Noonan Syndrome-like Developmental Disorder
Noonan Syndrome-like Disorder with Loose Anagen Hair 2
Nos3 Protein Levels
Npdc1 Protein Levels
Nrap-related Disorder
Nsfl1c Protein Levels
Nuclear Protein Mdm1 Levels
Nuclear Type 31
Ocia Domain-containing Protein 1 Levels
Ocrl-related Disorder
Oculocutaneous Albinism Type 6
Oculocutaneous Albinism Type 8
Oculogastrointestinal-neurodevelopmental Syndrome
Oguchi Disease-1
Oleoyl-linoleoyl-glycerol (18:1/18:2) [1] Levels in Elite Athletes
Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] Levels
Optic Atrophy 5
Optic Nerve Head Parameters (multi-trait Analysis)
Optic Nerve Measurement (disc Area)
Orofaciodigital Syndrome Xv
Osteocraniostenosis
Osteogenesis Imperfecta Type 16
Otc-related Disorder
Other Endocrine Disorders (phecode 259)
Other Immunological Findings (phecode 279.7)
Otu97_86 (phascolarctobacterium) Abundance
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