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Transition IssuesDiagnoses & ConditionsDiagnosis Prevalence ListOther Names for Diagnoses & ConditionsAnxiety Disorders & Attention Deficit Hyperactivity Disorder (ADHD)Angelman SyndromeAnxiety DisordersArginase DeficiencyAsthmaAttention-Deficit/Hyperactivity Disorder (ADHD)Autism Spectrum DisorderBiotinidase DeficiencyCeliac DiseaseCerebral PalsyCharcot-Marie-Tooth Disease (Hereditary Motor Sensory Neuropathy)Childhood Absence EpilepsyConstipationCornelia de Lange SyndromeCystic FibrosisDepressionDuchenne & Becker Muscular DystrophyDown SyndromeFabry DiseaseFetal Alcohol Spectrum DisordersFoster CareFragile X SyndromeGalactosemiaHeadache (Migraine & Chronic)Hearing Loss & DeafnessHomocystinuriaInfantile SpasmsIntellectual Disability & Global Developmental DelayLCHAD/TFP DeficiencyLeukodystrophiesMaple Syrup Urine Disease (MSUD)MCADDMucopolysaccharidosis Type I (MPS 1)Myotonic Muscular Dystrophy Type 1Neurofibromatosis Type 1Obesity in ChildrenObsessive-Compulsive Disorder (OCD)PKU & Pterin DefectsPostural Orthostatic Tachycardia Syndrome (POTS)Prader-Willi SyndromePremature Infant Follow-UpRett SyndromeSeizures/EpilepsySickle Cell DiseaseSpina BifidaSpinal Cord InjurySpinal Muscular AtrophySubstance Use DisordersTourette SyndromeTransgender & Gender-DiverseTraumatic Brain InjuryTuberous Sclerosis Complex (TSC)Turner Syndrome22q11.2 Deletion SyndromeTyrosinemia Type 1VLCADDXXY (Klinefelter) Syndrome
Newborn DisordersNewborn DisordersEfrain TestMCADD TestAdrenoleukodystrophy (ALD)ArgininemiaArgininosuccinic AciduriaBeta-Ketothiolase DeficiencyBiotinidase DeficiencyCACT & CPT II DeficienciesCarnitine Palmitoyltransferase 1A (CPT 1) DeficiencyCarnitine Uptake DefectCitrullinemia Type 1Citrullinemia Type II & Citrin DeficiencyCongenital Adrenal HyperplasiaCongenital HypothyroidismCritical Congenital Heart Disease (CCHD)Cystic FibrosisFabry DiseaseGalactosemiaGlutaric Acidemia Type 1Glutaric Acidemia Type 2Guanidinoacetate Methyltransferase (GAMT) DeficiencyHearing Loss & DeafnessHMG-CoA Lyase DeficiencyHolocarboxylase/Multiple Carboxylase DeficiencyHomocystinuria (Classic)Isobutyryl-CoA Dehydrogenase DeficiencyIsovaleric AcidemiaLCHAD/TFP DeficiencyMalonic AcidemiaMaple Syrup Urine DiseaseMedium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)Methylmalonic AcidemiasPhenylketonuria (PKU)Pompe DiseasePropionic AcidemiaPyruvate Carboxylase DeficiencySevere Combined Immunodeficiency (SCID)Short/Branched Chain Acyl-CoA Dehydrogenase DeficiencyShort-Chain Acyl-CoA Dehydrogenase Deficiency (SCADD)-DraftSickle Cell DiseaseSpinal Muscular Atrophy3MCC Deficiency3-Methylglutaconic Aciduria (3MGA)2M3HBA DeficiencyTyrosinemia Type 1VLCADD
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