Health Conditions

43,676 conditions with known genetic associations in our database.

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