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)
Nphp4-related Disorder
Phosphatidylcholine-o(38:5)_[m+h]1+/phosphatidylcholine-p(38:4)_[m+h]1+ Levels
Phosphatidylcholine(37:4)_[m+h]1+/phosphatidylethanolamine(40:4)_[m+h]1+/phosphatidate(42:5)_[m+nh4]1+ Levels
Pontine
Ptch1-related Disorder
Spondylometaphyseal Dysplasia - Sutcliffe Type
Tinnitus-related Distress
Type 2 Collagenopathy
Tyrosinemia Type Ii
Uterine Leiomyomata
Xcl1 Protein Levels
Abca4-related Retinopathy
Alcohol Use Disorder (consumption Score)
And Nail Dystrophy
Anterior Segment Dysgenesis 6
Autosomal Dominant Spastic Paraplegia Type 9
Cholesteryl Ester Levels in Idl
De Barsy Syndrome
Enpp5 Protein Levels
Epiphyseal Dysplasia
Flna-related Disorder
Gpc5 Protein Levels
Hereditary Spherocytosis Type 4
Il12b Protein Levels
Immunodeficiency 35
Mortality in Covid-19
Neuroticism Conditioned On Self-rated Math Ability (multi-trait Conditioning and Joint Analysis)
Neutrophil Forward Scatter
Nicolaides-baraitser Syndrome
Orbital Telorism
Parental Extreme Longevity (95 Years and Older)
Pityriasis Rubra Pilaris
Sirpa Protein Levels
T-cell Immunodeficiency
Vitamin D Levels or Covid-19 (mtag)
Afp Protein Levels
Astrocytoma
Ataxia - Intellectual Disability - Oculomotor Apraxia - Cerebellar Cysts Syndrome
Autosomal Dominant 14
Cacna1a-related Disorder
Charcot-marie-tooth Disease Type 1b
Cholesteryl Ester(20:5)_[m+nh4]1+ Levels
Cognitive Ability
Col6a3-related Disorder
Cortical Thickness (mostest)
Deficiency of Butyrylcholinesterase
Delayed Speech and Language Development
Diffuse
Experiencing Mood Swings
Gestational Length in Nulliparas
Glomerulopathy with Fibronectin Deposits 2
Large B-cell
Laryngo-onycho-cutaneous Syndrome
Monocyte Chemoattractant Protein-1 Levels
Neurological Blood Protein Biomarker Levels
Oculotrichoanal Syndrome
Pc2 of Congitive Measures
Peroxisome Biogenesis Disorder 7b
Phelan-mcdermid Syndrome
Red Blood Cell Distribution Width
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