]> 2026-08-01T18:44:11+00:00 Genetic disorders patient information 14 en 2011-07-27T14:22:55Z 2455770.0992477 Genetic disorders patient information Genetic counseling 0 en Genetic counseling Pericardial effusion (patient information) 0 en Pericardial effusion (patient information) Achondroplasia (patient information) 0 en Achondroplasia (patient information) Phenylketonuria (patient information) 0 en Phenylketonuria (patient information) Ataxia (patient information) 0 en Ataxia (patient information) Optic nerve glioma (patient information) 0 en Optic nerve glioma (patient information) Von Willebrand disease (patient information) 0 en Von Willebrand disease (patient information) Celiac disease (patient information) 0 en Celiac disease (patient information) Sickle-cell disease (patient information) 0 en Sickle-cell disease (patient information) Amblyopia (patient information) 0 en Amblyopia (patient information) Glycogen storage disease type III (patient information) 0 en Glycogen storage disease type III (patient information) Wilson's disease (patient information) 0 en Wilson's disease (patient information) Congenital protein C or S deficiency (patient information) 0 en Congenital protein C or S deficiency (patient information) Glycogen storage disease type II (patient information) 0 en Glycogen storage disease type II (patient information) Tay-Sachs disease (patient information) 0 en Tay-Sachs disease (patient information) Alagille syndrome (patient information) 0 en Alagille syndrome (patient information) Aarskog-Scott syndrome (patient information) 0 en Aarskog-Scott syndrome (patient information) Bartter syndrome (patient information) 0 en Bartter syndrome (patient information) Fragile X syndrome (patient information) 0 en Fragile X syndrome (patient information) Crigler-Najjar syndrome (patient information) 0 en Crigler-Najjar syndrome (patient information) Congenital hypothyroidism (patient information) 0 en Congenital hypothyroidism (patient information) Shwachman-Diamond syndrome (patient information) 0 en Shwachman-Diamond syndrome (patient information) Color blindness (patient information) 0 en Color blindness (patient information) Hereditary pancreatitis (patient information) 0 en Hereditary pancreatitis (patient information) IgA nephropathy (patient information) 0 en IgA nephropathy (patient information) Klinefelter's syndrome (patient information) 0 en Klinefelter's syndrome (patient information) Ichthyosis vulgaris (patient information) 0 en Ichthyosis vulgaris (patient information) Menkes disease (patient information) 0 en Menkes disease (patient information) Adrenoleukodystrophy (patient information) 0 en Adrenoleukodystrophy (patient information) Alkaptonuria (patient information) 0 en Alkaptonuria (patient information) Myotonia congenita (patient information) 0 en Myotonia congenita (patient information) Costello syndrome (patient information) 0 en Costello syndrome (patient information) Down syndrome (patient information) 0 en Down syndrome (patient information) Cri du chat (patient information) 0 en Cri du chat (patient information) Edwards syndrome (patient information) 0 en Edwards syndrome (patient information) Patau syndrome (patient information) 0 en Patau syndrome (patient information) Turner syndrome (patient information) 0 en Turner syndrome (patient information) Prader-Willi syndrome (patient information) 0 en Prader-Willi syndrome (patient information) Spinal muscular atrophy (patient information) 0 en Spinal muscular atrophy (patient information) Niemann-Pick disease (patient information) 0 en Niemann-Pick disease (patient information) Lesch-Nyhan's syndrome (patient information) 0 en Lesch-Nyhan's syndrome (patient information) Homocystinuria (patient information) 0 en Homocystinuria (patient information) Glycogen storage disease type I (patient information) 0 en Glycogen storage disease type I (patient information) Hereditary elliptocytosis (patient information) 0 en Hereditary elliptocytosis (patient information) Gaucher's disease (patient information) 0 en Gaucher's disease (patient information) Paroxysmal nocturnal hemoglobinuria (patient information) 0 en Paroxysmal nocturnal hemoglobinuria (patient information) Alpha 1-antitrypsin deficiency (patient information) 0 en Alpha 1-antitrypsin deficiency (patient information) Neuronal ceroid lipofuscinosis (patient information) 0 en Neuronal ceroid lipofuscinosis (patient information) Urea cycle disorder (patient information) 0 en Urea cycle disorder (patient information) Mucopolysaccharidosis (patient information) 0 en Mucopolysaccharidosis (patient information) Maple syrup urine disease (patient information) 0 en Maple syrup urine disease (patient information) Rett syndrome (patient information) 0 en Rett syndrome (patient information) Canavan disease (patient information) 0 en Canavan disease (patient information) Cerebral palsy (patient information) 0 en Cerebral palsy (patient information) Amyotrophic lateral sclerosis (patient information) 0 en Amyotrophic lateral sclerosis (patient information) Huntington's disease (patient information) 0 en Huntington's disease (patient information) Ataxia telangiectasia (patient information) 0 en Ataxia telangiectasia (patient information) Craniosynostosis (patient information) 0 en Craniosynostosis (patient information) Polycystic kidney disease (patient information) 0 en Polycystic kidney disease (patient information) Hypertriglyceridemia (patient information) 0 en Hypertriglyceridemia (patient information) Lesch-Nyhan syndrome (patient information) 0 en Lesch-Nyhan syndrome (patient information) Phosphate nephropathy (patient information) 0 en Phosphate nephropathy (patient information) Post-streptococcal glomerulonephritis (patient information) 0 en Post-streptococcal glomerulonephritis (patient information) Pyonephrosis (patient information) 0 en Pyonephrosis (patient information) Rapidly progressive glomerulonephritis (patient information) 0 en Rapidly progressive glomerulonephritis (patient information) Renal agenesis (patient information) 0 en Renal agenesis (patient information) Renal osteodystrophy (patient information) 0 en Renal osteodystrophy (patient information) Aarskog-Scott syndrome (patient information) 0 en Aarskog-Scott syndrome (patient information) Achondroplasia (patient information) 0 en Achondroplasia (patient information) Adrenoleukodystrophy (patient information) 0 en Adrenoleukodystrophy (patient information) Alagille syndrome (patient information) 0 en Alagille syndrome (patient information) Alkaptonuria (patient information) 0 en Alkaptonuria (patient information) Alpha 1-antitrypsin deficiency (patient information) 0 en Alpha 1-antitrypsin deficiency (patient information) Amblyopia (patient information) 0 en Amblyopia (patient information) Amyotrophic lateral sclerosis (patient information) 0 en Amyotrophic lateral sclerosis (patient information) Ataxia (patient information) 0 en Ataxia (patient information) Ataxia telangiectasia (patient information) 0 en Ataxia telangiectasia (patient information) Bartter syndrome (patient information) 0 en Bartter syndrome (patient information) Canavan disease (patient information) 0 en Canavan disease (patient information) Celiac disease (patient information) 0 en Celiac disease (patient information) Cerebral palsy (patient information) 0 en Cerebral palsy (patient information) Color blindness (patient information) 0 en Color blindness (patient information) Congenital hypothyroidism (patient information) 0 en Congenital hypothyroidism (patient information) Congenital protein C or S deficiency (patient information) 0 en Congenital protein C or S deficiency (patient information) Costello syndrome (patient information) 0 en Costello syndrome (patient information) Craniosynostosis (patient information) 0 en Craniosynostosis (patient information) Cri du chat (patient information) 0 en Cri du chat (patient information) Crigler-Najjar syndrome (patient information) 0 en Crigler-Najjar syndrome (patient information) Down syndrome (patient information) 0 en Down syndrome (patient information) Edwards syndrome (patient information) 0 en Edwards syndrome (patient information) Fragile X syndrome (patient information) 0 en Fragile X syndrome (patient information) Gaucher's disease (patient information) 0 en Gaucher's disease (patient information) Genetic counseling 0 en Genetic counseling Glycogen storage disease type I (patient information) 0 en Glycogen storage disease type I (patient information) Glycogen storage disease type II (patient information) 0 en Glycogen storage disease type II (patient information) Glycogen storage disease type III (patient information) 0 en Glycogen storage disease type III (patient information) Hereditary elliptocytosis (patient information) 0 en Hereditary elliptocytosis (patient information) Hereditary pancreatitis (patient information) 0 en Hereditary pancreatitis (patient information) Homocystinuria (patient information) 0 en Homocystinuria (patient information) Huntington's disease (patient information) 0 en Huntington's disease (patient information) Hypertriglyceridemia (patient information) 0 en Hypertriglyceridemia (patient information) Ichthyosis vulgaris (patient information) 0 en Ichthyosis vulgaris (patient information) IgA nephropathy (patient information) 0 en IgA nephropathy (patient information) Klinefelter's syndrome (patient information) 0 en Klinefelter's syndrome (patient information) Lesch-Nyhan syndrome (patient information) 0 en Lesch-Nyhan syndrome (patient information) Lesch-Nyhan's syndrome (patient information) 0 en Lesch-Nyhan's syndrome (patient information) Maple syrup urine disease (patient information) 0 en Maple syrup urine disease (patient information) Menkes disease (patient information) 0 en Menkes disease (patient information) Mucopolysaccharidosis (patient information) 0 en Mucopolysaccharidosis (patient information) Myotonia congenita (patient information) 0 en Myotonia congenita (patient information) Neuronal ceroid lipofuscinosis (patient information) 0 en Neuronal ceroid lipofuscinosis (patient information) Niemann-Pick disease (patient information) 0 en Niemann-Pick disease (patient information) Optic nerve glioma (patient information) 0 en Optic nerve glioma (patient information) Paroxysmal nocturnal hemoglobinuria (patient information) 0 en Paroxysmal nocturnal hemoglobinuria (patient information) Patau syndrome (patient information) 0 en Patau syndrome (patient information) Pericardial effusion (patient information) 0 en Pericardial effusion (patient information) Phenylketonuria (patient information) 0 en Phenylketonuria (patient information) Phosphate nephropathy (patient information) 0 en Phosphate nephropathy (patient information) Polycystic kidney disease (patient information) 0 en Polycystic kidney disease (patient information) Post-streptococcal glomerulonephritis (patient information) 0 en Post-streptococcal glomerulonephritis (patient information) Prader-Willi syndrome (patient information) 0 en Prader-Willi syndrome (patient information) Pyonephrosis (patient information) 0 en Pyonephrosis (patient information) Rapidly progressive glomerulonephritis (patient information) 0 en Rapidly progressive glomerulonephritis (patient information) Renal agenesis (patient information) 0 en Renal agenesis (patient information) Renal osteodystrophy (patient information) 0 en Renal osteodystrophy (patient information) Rett syndrome (patient information) 0 en Rett syndrome (patient information) Shwachman-Diamond syndrome (patient information) 0 en Shwachman-Diamond syndrome (patient information) Sickle-cell disease (patient information) 0 en Sickle-cell disease (patient information) Spinal muscular atrophy (patient information) 0 en Spinal muscular atrophy (patient information) Tay-Sachs disease (patient information) 0 en Tay-Sachs disease (patient information) Turner syndrome (patient information) 0 en Turner syndrome (patient information) Urea cycle disorder (patient information) 0 en Urea cycle disorder (patient information) Von Willebrand disease (patient information) 0 en Von Willebrand disease (patient information) Wilson's disease (patient information) 0 en Wilson's disease (patient information) INST 102 en INST