| Document Date: 2012-02-06 15:20:30
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Continent Africa / / Country India / / IndustryTerm enzyme systems / / MedicalCondition alpha-thalassemia / strokes / Congenital Adrenal Hyperplasia / seizures / Sickle cell anemia / bronchitis / coma / deletion alpha thalassemia / Disorder / Deficiency Marker Analyte Congenital Hypothyroidism / beta thalassemia minor / muscle weakness / severe hypothyroidism / Galactosemia / severe anemia / clinically important thalassemias / disorder / diarrhea / mild hemolytic anemia / Thalassemia / autosomal recessive disorder / Cystic Fibrosis / hearing loss / liver disease / infections / thalassemias / wheezing / E disease / ataxia / Hemoglobinopathies / pneumonia / mental retardation / cancer / cataracts / Beta thalassemias / shortness of breath / lung infections / Metabolic acidosis / beta-thalassemia resulting / eczema / coughing / slight anemia / Cooley's anemia / congenital deficiency / C disease / lethargy / vomiting / pain / Cell Anemia The sickle cell mutation / frequent infections / sickle cell disease / beta thalassemia major / seborrheic dermatitis / infection / hypotonia / sickle cell trait / deficiency / G Hemoglobinopathies / Biotinidase Deficiency / serious bacterial infections / anemia / meconium ileus / disorders / influenza B / mild anemia / genetic disorders / dehydration / / MedicalTreatment blood transfusion / blood transfusions / vaccinations / / Organization Harvard / Cell Information Center / / Person Gene InPlexTM / James Eckman / / Product penicillin / / RadioStation CFTR / / Region Southeast Asia / Mediterranean / / Technology alpha / / URL http /
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Disorder / Deficiency Marker Analyte Congenital Hypothyroidism (CH)