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)
Type Viib
Abnormal Facial Shape
Age At Natural Menopause
Amyotrophic Lateral Sclerosis Type 6
Autosomal Dominant 50
Autosomal Recessive 6
Autosomal Recessive Congenital Ichthyosis 5
Autosomal Recessive Multiple Pterygium Syndrome
Body Mass Index Z-score
Cd101 Protein Levels
Cfi-related Disorder
Chloride (maximum, Inv-norm Transformed)
Cholesteryl Esters in Ldl
Corpus Callosum Central Posterior Subregion Volume
Cxcl6 Protein Levels
Dystonia 9
Ear Malformation
Emery-dreifuss Muscular Dystrophy 2
Familial Thoracic 6
Fcrl1 Protein Levels
Gnly Protein Levels
Gut Microbial Network Clusters (salmon (at 1 Year) X Spring Birth (mar-may) Interaction
Hereditary Spastic Paraplegia 50
Idiopathic Hypereosinophilic Syndrome
Il17ra Protein Levels
Immunoglobulin A Vasculitis
Ly9 Protein Levels
Nonsyndromic Orofacial Cleft X Sex Interaction (2df)
Obp2b Protein Levels
Phosphatidate(43:4)_[m-h]1- Levels
Phosphatidylcholine-o(36:1)_[m+h]1+/phosphatidylethanolamine-o(39:1)_[m+h]1+/phosphatidylcholine-p(36:0)_[m+h]1+ Levels
Phosphatidylinositol-o(36:0)_[m-h]1-/phosphatidylglycerol(37:0)_[m+oac]1- Levels
Phytanic Acid Storage Disease
Plb1 Protein Levels
Refractive Astigmatism
Response to Antipsychotic Treatment
Severe Infantile Type
Sialic Acid Storage Disease
Sphingomyelin(42:4)_[m+h]1+ Levels
Triglycerides X Depression Interaction (2df Test)
Turner Type
Vitamin D-dependent Rickets
With Impaired Proprioception and Touch
X-linked Syndromic
2-aminoadipic 2-oxoadipic Aciduria
Abcb4-related Disorder
Acp6 Protein Levels
Anterior Segment Dysgenesis
Anti-hepatitis E Antibody Levels
Apoe Protein Levels
Astrocytoma (low-grade)
Autosomal Recessive 13
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2t
Bone Mineral Density (femoral Neck)
Catecholaminergic Polymorphic Ventricular Tachycardia 2
Cd207 Protein Levels
Cd300c Protein Levels
Cd5l Protein Levels
Cog7 Congenital Disorder of Glycosylation
Cognitive Impairment with or Without Cerebellar Ataxia
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →