Metabolism, Inborn ErrorsLipid MetabolismLipidsAmino Acid Metabolism, Inborn ErrorsLipid Metabolism, Inborn ErrorsLipid ANeonatal ScreeningSteroid Metabolism, Inborn ErrorsPurine-Pyrimidine Metabolism, Inborn ErrorsLipid Metabolism DisordersLiverCarbohydrate Metabolism, Inborn ErrorsEnergy MetabolismFatty AcidsTriglyceridesLipid BilayersUrea Cycle Disorders, InbornCholesterolBrain Diseases, Metabolic, InbornBipolar DisorderArgininosuccinic AciduriaHyperammonemiaLipid PeroxidationMental DisordersPhenylketonuriasMutationAnxiety DisordersMood DisordersSmith-Lemli-Opitz SyndromeGlucosePhospholipidsInfant, NewbornMetabolic DiseasesCarnitineMolecular Sequence DataRefractive ErrorsAdipose TissueHomogentisate 1,2-DioxygenaseLipid PeroxidesDiagnostic and Statistical Manual of Mental Disordersalpha-GalactosidaseHomocystinuriaCandidiasis, Chronic MucocutaneousFabry DiseaseTime FactorsPyruvate Metabolism, Inborn ErrorsModels, BiologicalPhenotypeFatty Acids, NonesterifiedMetabolic Networks and PathwaysOrnithine Carbamoyltransferase Deficiency DiseaseAustralian Capital TerritoryMetabolismOxidation-ReductionInsulinArgininosuccinic AcidBlood GlucoseDiagnostic ErrorsIsovaleryl-CoA DehydrogenaseHypophosphatasiaBrain Diseases, MetabolicBrainMagnetic Resonance SpectroscopyDietary FatsGene Expression RegulationMethylmalonic AcidLipoproteinsPPAR alphaPentanoic AcidsBody WeightOxidoreductases Acting on CH-CH Group DonorsHydroxocobalaminLipolysisMice, KnockoutDepressive Disorder, MajorMethylmalonyl-CoA MutaseMice, Inbred C57BLMetal Metabolism, Inborn ErrorsAttention Deficit Disorder with HyperactivityGlutaratesSterol Regulatory Element Binding Protein 1Insulin ResistanceLipogenesisCells, CulturedBase SequenceIron Metabolism DisordersRNA, MessengerFructose Metabolism, Inborn ErrorsGene Expression ProfilingPedigreeMass SpectrometryMaple Syrup Urine DiseaseObesityPhosphatidylcholinesDepressive DisorderRare DiseasesSignal TransductionAmidinotransferasesAmino Acid SequenceReceptors, Cytoplasmic and Nuclear