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)
Oculocutaneous Albinism Type 1a
144 variants Other
Pigmentary Pallidal Degeneration
144 variants Other
Cataracts
143 variants Other
Gut Microbial Network Clusters (purple (at 1 Year) X Household Furry Pet Cat (3 Months) Interaction
143 variants Other
Hepatoencephalopathy Due to Combined Oxidative Phosphorylation Defect Type 1
143 variants Other
Loeys-dietz Syndrome 2
143 variants Other
Long Qt Syndrome 3
143 variants Other
Neutrophil-to-lymphocyte Ratio
143 variants Other
Recessive
143 variants Other
Thymoma
143 variants Other
Triglycerides in Very Large Hdl
143 variants Other
Autosomal Recessive Retinitis Pigmentosa
142 variants Other
Baseline Memory in Normal Cognition X Sex Interaction
142 variants Other
Cone-rod Dystrophy 13
142 variants Other
Fg Syndrome
142 variants Other
Pierson Syndrome
142 variants Other
Short-rib Thoracic Dysplasia 6 with or Without Polydactyly
142 variants Other
Triglycerides in Ldl
142 variants Other
Type Ia
142 variants Other
Ataxia
141 variants Other
Cholesteryl Esters in Small Hdl
141 variants Other
Danon Disease
141 variants Other
Dilated Cardiomyopathy 1s
141 variants Other
Neuronal Ceroid Lipofuscinosis 7
141 variants Other
Plec-related Disorder
141 variants Other
Alg6-congenital Disorder of Glycosylation 1c
140 variants Other
Covid-19 (hospitalized Vs Not Hospitalized)
140 variants Other
Kyphoscoliotic Type 1
140 variants Other
Lymphocyte (fraction, Mean, Inv-norm Transformed)
140 variants Other
Opioid Addiction
140 variants Other
Perlman Syndrome
140 variants Other
Pyruvate Dehydrogenase E1-alpha Deficiency
140 variants Other
Blood Glucose Levels
139 variants Other
Cataract 41
139 variants Other
Childhood Hypophosphatasia
139 variants Other
Corpus Callosum Posterior Subregion Volume
139 variants Other
Due to Adenosine Deaminase Deficiency
139 variants Other
Elliptocytosis 2
139 variants Other
Hereditary Spastic Paraplegia 48
139 variants Other
Neuroticism General Factor
139 variants Other
Nk Cell-negative
139 variants Other
T-b+ Severe Combined Immunodeficiency Due to Jak3 Deficiency
139 variants Other
Autosomal Recessive Congenital Ichthyosis 2
138 variants Other
Cbla Type
138 variants Other
Congenital Myopathy 18
138 variants Other
Cortical Surface Area (mostest)
138 variants Other
Memory Decline X Sex Interaction
138 variants Other
Ocular Cystinosis
138 variants Other
Urea Levels (ukb Data Field 30670)
138 variants Other
Autosomal Dominant Cerebellar Ataxia
137 variants Other
Cognitive Function (baseline)
137 variants Other
Facioscapulohumeral Muscular Dystrophy 2
137 variants Other
Hermansky-pudlak Syndrome
137 variants Other
Neonatal-onset Encephalopathy with Rigidity and Seizures
137 variants Other
Spongy Degeneration of Central Nervous System
137 variants Other
Telomere Length
137 variants Other
Thrombophilia
137 variants Other
Congenital Muscular Dystrophy Due to Partial Lama2 Deficiency
136 variants Other
Eosinophil (fraction, Minimum, Inv-norm Transformed)
136 variants Other
Malaria
136 variants Other
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