A laboratory test result indicating elevated triglyceride concentration in the blood.
Známé také jako
hypertriglyceridemia (disease)
Zahrnuje 2 příbuzných podtypů ↓Skrýt podtypy ↑
- hypertriglyceridemia 1
- hypertriglyceridemia 2
Co vaše zpráva obsahuje
Onemocnění, které analyzujeme
Další metabolic conditions
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)SMPD1
- AlkaptonuriaHGD
- Alpha-Mannosidosis and Other GlycoproteinosesAGA, CTSA, FUCA1, MAN2B1
- BH4 Deficiency & Monoamine Neurotransmitter DisordersDBH, DDC, DNAJC12, GCH1
- Beta-ureidopropionase deficiencyUPB1
- Biotinidase & Holocarboxylase DeficiencyBTD, HLCS
- Cerebral Creatine Deficiency SyndromesGAMT, GATM, SLC6A8
- CitrullinemiaASS1, SLC25A13
- Classic Organic AciduriasACAT1, GCDH, HMGCL, IVD
- Congenital Disorders of GlycosylationA4GALT, ALG1, ALG11, ALG12
- CystinosisCTNS
- Danon DiseaseLAMP2
- Diabetes MellitusABCC8, AKT2, APPL1, BSCL2
- Disorder of Copper MetabolismAP1S1, ATP7A, ATP7B
- Disorders of Glycine & Serine MetabolismAMT, GCSH, GLDC, PHGDH
- Fabry DiseaseGLA
- Familial HypercholesterolemiaAPOB, LDLR, LDLRAP1, PCSK9
- Fatty Acid Oxidation & Carnitine Cycle DisordersACAD9, ACADM, ACADS, ACADVL
- GM1 Gangliosidosis and Morquio B SyndromeGLB1
- GPI Anchor Biosynthesis DefectsGPAA1, PGAP2, PGAP3, PIGA
- GalactosemiaGALE, GALK1, GALM, GALT
- Gaucher DiseaseGBA1
- Gilbert SyndromeABCC2, UGT1A1
- Glutathione Synthetase DeficiencyGSS
- Glycogen Storage DiseaseAGL, ENO3, G6PC1, GBE1
- HemochromatosisCYBRD1, HAMP, HFE, HJV
- Hepatic Porphyria DisordersALAD, ALAS2, CLPX, CPOX
- Hereditary AmyloidosisAPOA1, APOA4, APP, B2M
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsALDOB, FBP1, PCK1
- Hereditary HypolipoproteinemiasABCA1, ANGPTL3, APOA1, APOB
- Hermansky-Pudlak SyndromeAP3B1, AP3D1, BLOC1S3, BLOC1S5
- Homocystinuria & Cobalamin DisordersABCD4, AHCY, AMN, CBLIF
- Hypercalcemia InfantileCYP24A1, SLC34A1
- HyperlipidemiaABCG5, ABCG8, APOA5, APOB
- HypophosphatasiaALPL
- LipodystrophyAGPAT2, AKT2, BSCL2, CAV1
- Lysosomal Acid Lipase Deficiency (Wolman Disease and CESD)LIPA
- Lysosomal Storage DiseaseABHD5, AGA, AP5Z1, ARSA
- Maple Syrup Urine DiseaseBCKDHA, BCKDHB, DBT, DLD
- McArdle's diseasePYGM
- Methylmalonic & Propionic AcidemiaABCD4, ACSF3, CD320, HCFC1
- Mucolipidoses (ML II, ML III and ML IV)GNPTAB, GNPTG, MCOLN1
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)IDUA
- Mucopolysaccharidosis Type II (Hunter Syndrome)IDS
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)GNS, HGSNAT, NAGLU, SGSH
- Mucopolysaccharidosis Type IVA (Morquio A Syndrome)GALNS
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)ARSB
- Mucopolysaccharidosis Type VII (Sly Syndrome)GUSB
- Myalgic Encephalomyelitis / Chronic Fatigue Syndrome
- Niemann-Pick Disease Type CNPC1, NPC2
- Peroxisomal Enzyme Disorders & Refsum DiseaseACOX1, AGPS, AMACR, GNPAT
- Phenylketonuria (PKU)PAH
- Pompe DiseaseGAA
- PorphyriaALAD, ALAS2, CLPX, CPOX
- Primary HyperoxaluriaAGXT, GRHPR, HOGA1
- Primary Mitochondrial DiseaseAARS2, ACAD9, AFG3L2, AGK
- Purine & Pyrimidine Metabolism DisordersADSL, APRT, DPYD, DPYS
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyDLAT, DLD, LIAS, MPC1
- Salla Disease and Free Sialic Acid Storage DiseaseSLC17A5
- Sandhoff Disease and GM2 Activator DeficiencyGM2A, HEXB
- Tay-Sachs DiseaseHEXA
- TrimethylaminuriaFMO3
- TyrosinemiaFAH, HPD, TAT
- Urea Cycle DisorderARG1, ASL, ASS1, CA5A
- Very Long Chain Acyl-Coa Dehydrogenase DeficiencyACADVL
- Wilson DiseaseATP7B
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