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Newborn screening / Congenital adrenal hyperplasia / Galactosemia / Phenylketonuria / Biotinidase deficiency / Congenital hypothyroidism / 3-Methylcrotonyl-CoA carboxylase deficiency / Inborn error of metabolism / 2-Methylbutyryl-CoA dehydrogenase deficiency / Health / Medicine / Pediatrics


Title 15 - Mississippi Department of Health
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Document Date: 2014-03-27 09:48:48


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File Size: 102,47 KB

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Country

United States / /

Facility

College of American Pathologists / /

IndustryTerm

state law / energy / biochemical and other established technologies / State law exempts / /

MedicalCondition

Methylcrotonyl-CoA Carboxylase Deficiency / Short-Chain Acyl-CoA Dehydrogenase Deficiency / Homocitrullinemia Dehydrogenase Deficiency / Trifunctional Protein Deficiency / congenital adrenal hyperplasia / organic acid disorders / Mitochondrial Acetoacetyl-CoA Thiolase Deficiency / CoA Lyase Deficiency / Acyl- CoA Dehydrogenase Deficiency / another birth defect / seizures / Reportable Birth Defects / each disorder / sickle cell anemia / hereditary condition / severe mental retardation / ASA Synthetase Deficiency / coma / CPS Deficiency / Citrullinemia / CoA Hydratase Deficiency / Long-Chain Acyl-CoA Dehydrogenase Deficiency / II Deficiency / galactosemia / Streptococcus pneumonia / Carbamoylphosphate Synthetase Deficiency / birth defect / disorder / amino acid disorders / thalassemia / phenylketonuria / MEDIUM CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY / Cystic Fibrosis / hearing loss / hypoglycemia / Reportable Fetal Deaths / birth defects / Homocystinuria / diagnosed birth defect / hemoglobinopathies / Medium-Chain Acyl-CoA Dehydrogenase Deficiency / sickle cell diseases / Acyl-CoA Dehydrogenase Deficiency / mental retardation / I Deficiency / CoA Dehydrogenase Deficiency / Respiratory failure / common hemoglobinopathy / hypothyroidism / hemoglobinopathy / TFP Deficiency / every birth defect / Argininemia / genetic disorder / eczema / Short-Chain Hydroxy Acyl-CoA Dehydrogenase Deficiency / nutritional deficiencies / congenital hypothyroidism / fatty acid disorders / genetic endocrine disorder / lethargy / vomiting / cut / inherited disease / Carnitine/Acylcarnitine Translocase Deficiency / certain principal birth defects / fetal death / PKU / sickle cell disease / Infection / sickle cell trait / deficiency / Biotinidase Deficiency / ASA Lyase Deficiency / Cell Disease / Isobutyryl-CoA Dehydrogenase Deficiency / Maple Syrup Urine Disease / Syndrome / Disorders / apnea / cardiac arrest / congenital adrenal hyperplasia screening / genetic disorders / /

Organization

College of American Pathologists / MADD / Mississippi Department / Medicare / State Board of Health / American Association of Clinical Chemists / Genetics Chapter / FDA / office of Health Services Subpart / Statutory Authority / Department of Health / /

Position

State Health Officer / The State Health Officer / physician / /

ProvinceOrState

Mississippi / /

Region

Mediterranean / /

SocialTag