The Health Report analyzes predispositions to common diseases caused by your genetic variants.
The predispositions analyzed are 74:
- Andermann Syndrome
- Arrhythmogenic Right Ventricular
- Cardiomyopathy
- Beta Thalassemia
- Bloom Syndrome
- Brugada Syndrome
- Canavan Disease
- Catecholaminergic Polymorphic
- Ventricular Tachycardia
- Cystic Fibrosis
- D-Bifunctional Protein Deficiency
- Dihydrolipoamide Dehydrogenase
- Deficiency
- Dilated Cardiomyopathy
- Ehlers-Danlos Syndrome
- Fabry Disease
- Familial Adenomatous Polyposis
- Familial Dysautonomia
- Familial Hypercholesterolemia
- Familial Hyperinsulinism
- Familial Hypertrophic Cardiomyopathy
- Familial Thoracic Aortic Aneurysm And Dissection
- Fanconi Anemia
- Gaucher Disease
- Glycogen Storage Disease Type I
- Gracile Syndrome
- Hereditary Fructose Intolerance
- Junctional Epidermolysis Bullosa
- Juvenile Polyposis Syndrome
- Left Ventricular Noncompaction
- Leigh Syndrome
- Li-Fraumeni Syndrome
- Limb-Girdle Muscular Dystrophy
- Loeys-Dietz Syndrome
- Long Qt Syndrome
- Malignant Hyperthermia
- Maple Syrup Urine Disease
- Marfan Syndrome
- Medium-Chain Acyl-Coenzyme A
- Dehydrogenase Deficiency
- Mucolipidosis Type Iv
- Neurofibromatosis Type 2
- Neuronal Ceroid Lipofuscinosis Cln1 Related
- Neuronal Ceroid Lipofuscinosis Cln5 Related
- Niemann-Pick Disease Type A
- Nijmegen Breakage Syndrome
- Nonsyndromic Hearing Loss And Deafness Gjb2 Related
- Ornithine Transcarbamylase Deficiency
- Paragangliomas
- Pendred Syndrome
- Peutz-Jeghers Syndrome
- Phenylketonuria
- Pilomatrixoma
- Pmm2-Congenital Disorder Of Glycosylation
- Polycystic Kidney Disease
- Pten Hamartoma Tumor Syndrome
- Tuberous Sclerosis
- Von Hippel-Lindau Syndrome
- Wilson Disease
- Primary Hyperoxaluria
- Rhizomelic Chondrodysplasia Punctata
- Sialic Acid Storage Disease
- Sickle Cell Disease
- Sjögren-Larsson Syndrome
- Tay-Sachs Disease
- Tyrosinemia
- Usher Syndrome Type I
- Zellweger Spectrum Disorder
- Age-Related Macular Degeneration
- Hereditary Hemochromatosis
- Factor V Leiden Thrombophilia
- Prothrombin Thrombophilia
- Alpha-1 Antitrypsin Deficiency
- Glucose-6-Phosphate Dehydrogenase Deficiency