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)
Ige Levels
Igg N-glycosylation Phenotypes (multivariate Analysis)
Il10 Levels
Il18 Levels
Immunoglobulin-mediated Membranoproliferative Glomerulonephritis
Initial Pursuit Acceleration in Psychotic Disorders
Intellectual Disability and Myopathy Syndrome
Intercellular Adhesion Molecule 5 Levels
Isolated Coronal Synostosis
Itga11 Protein Levels
Itgam Protein Levels
Joubert Syndrome 32
Kif1b-related Disorder
Krit1-related Disorder
Lama5-related Disorder
Lambdoidal Craniosynostosis
Lamc3-related Disorder
Late-infantile Neuronal Ceroid Lipofuscinosis
Left Ventricular End Diastolic Volume (indexed to Body Surface Area)
Lewy Body Disease
Lumbar Spine Bone Mineral Density (integral)
Lypd8 Protein Levels
Maximum Cranial Width
Mcam Protein Levels
Metabolite Levels (dihydroxy Docosatrienoic Acid)
Metabolite Levels (mhpg)
Mhc Class Ii Deficiency 1
Mirror Movements 1
Mitochondrial Heteroplasmy Measurement
Mitochondrial Neurogastrointestinal Encephalomyopathy
Monohexosylceramide (d18:1/24:0) Levels
Mpo Protein Levels
Myh6-related Disorder
Myo-inositol Levels
N-glycan Levels
Nagpa Protein Levels
Nefh-related Disorder
Neurodevelopmental Disorder with Dysmorphic Facies and Distal Skeletal Anomalies
Neutrophil Side Scatter Distribution Width
Nod2-related Disorder
Nonsyndromic Ocular
Noonan Syndrome with Multiple Lentigines
Nthl1-related Disorder
Nuclear Type 21
Opioid Dependence
Ossification of the Posterior Longitudinal Ligament of the Spine
Overgrowth Syndrome And/or Cerebral Malformations Due to Abnormalities in Mtor Pathway Genes
Pain Intensity (nrs Pain Scale 1-11)
Palmoplantar Keratoderma-deafness Syndrome
Pappa Protein Levels
Parsopercularis Area
Penk Protein Levels
Perching Syndrome
Periodontal Disease
Peroxisome Biogenesis Disorder 13a (zellweger)
Pex5-related Disorder
Phosphatidylcholine-o(38:4)_[m+h]1+/phosphatidylcholine-p(38:3)_[m+h]1+ Levels
Phosphatidylethanolamine (18:1_18:1) Levels
Phosphatidylethanolamine_37:2_[m-h]1- Levels
Pik3ip1 Protein Levels
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