Merkmal
Elevated creatinine
Klinische Bezeichnung: Elevated circulating creatinine concentration
An increased amount of creatinine in the blood.
Zusammenfassung
- Auch genannt
- High blood creatinine level, Increased creatinine, Increased serum creatinine, Elevated serum creatinine
- Körpersystem
- Laboratory abnormality
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page$trait$nameLesen Sie die Gene aus, die mit Elevated creatinine zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
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Meinen Genome Test bestellen55 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Polycystic Kidney DiseaseReads 9 of these genesALG8IFT140ALG5ALG9DNAJB11GANABAbout this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 7 of these genesC3CD46CFBCFHCFIFAN1About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 4 of these genesSEC61A1UMODHNF1BMUC1About this report →
- Congenital Thrombotic Thrombocytopenic PurpuraReads 1 of these genesADAMTS13About this report →
Show 51 more reports
- CystinosisReads 1 of these genesCTNSAbout this report →
- Hand-Foot-Genital SyndromeReads 1 of these genesHOXA13About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 4 of these genesWDR19NEK8NPHP1INVSAbout this report →
- Hereditary SpherocytosisReads 2 of these genesSLC4A2SLC4A1About this report →
- Purine & Pyrimidine Metabolism DisordersReads 2 of these genesAPRTHPRT1About this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Renal HypouricemiaReads 1 of these genesSLC22A12About this report →
- MedulloblastomaReads 1 of these genesELP1About this report →
- Other Inborn Errors of ImmunityReads 8 of these genesSEC61A1TREX1C3CD46CFBCFHAbout this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesALG8About this report →
- Inherited Complement and Properdin DeficienciesReads 2 of these genesC3CFIAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- ThalassaemiaReads 1 of these genesHBBAbout this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A1About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR19About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesTREX1About this report →
- GlomerulosclerosisReads 1 of these genesPAX2About this report →
- PolycythemiaReads 1 of these genesHBBAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesSLC4A1About this report →
- ThrombophiliaReads 1 of these genesTHBDAbout this report →
- Joubert Syndrome And Related DisordersReads 2 of these genesCC2D2ANPHP1About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesSEC61A1About this report →
- Familial Intrahepatic CholestasisReads 1 of these genesPSKH1About this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesPAX2About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesDBHAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesPAX2About this report →
- Familial HypomagnesemiaReads 1 of these genesCLDN16About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF1BAbout this report →
- Type I InterferonopathiesReads 1 of these genesTREX1About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Retinitis PigmentosaReads 2 of these genesCC2D2AIFT140About this report →
- Neonatal Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Autoimmune DiseaseReads 1 of these genesTREX1About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesELP1About this report →
- Syndromic CraniosynostosisReads 1 of these genesWDR19About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesALG8ALG9About this report →
- Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesADAMTS13About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesTREX1About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesCC2D2ATREX1COQ7About this report →
- DNA Repair DiseaseReads 1 of these genesFAN1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesCC2D2AAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesCOQ7ELP1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesCTNSAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesCOQ7About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREX1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesCOQ7About this report →
Lesen Sie die Gene aus, die mit Elevated creatinine zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
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Meinen Genome Test bestellen56 Gene mit Elevated creatinine verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Elevated creatinine auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ALG8ALG8 alpha-1,3-glucosyltransferase | Immer | In 1 Erkrankung |
| APRTadenine phosphoribosyltransferase | Immer | In 1 Erkrankung |
| C1GALT1C1C1GALT1 specific chaperone 1 | Immer | In 1 Erkrankung |
| CC2D2Acoiled-coil and C2 domain containing 2A | Immer | In 1 Erkrankung |
| CLDN16claudin 16 | Immer | In 1 Erkrankung |
| CPT2carnitine palmitoyltransferase 2 | Immer | In 1 Erkrankung |
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Immer | In 1 Erkrankung |
| HOXA13homeobox A13 | Immer | In 1 Erkrankung |
| IFT140intraflagellar transport 140 | Immer | In 2 Erkrankungen |
| MLIPmuscular LMNA interacting protein | Immer | In 1 Erkrankung |
| PAX2paired box 2 | Immer | In 1 Erkrankung |
| PLD4phospholipase D family member 4 | Immer | In 1 Erkrankung |
| PSKH1protein serine kinase H1 | Immer | In 1 Erkrankung |
| SEC61A1SEC61 translocon subunit alpha 1 | Immer | In 1 Erkrankung |
| SLC41A1solute carrier family 41 member 1 | Immer | In 1 Erkrankung |
| SLC4A2solute carrier family 4 member 2 | Immer | In 1 Erkrankung |
| TMEM260transmembrane protein 260 | Immer | In 1 Erkrankung |
| WDR19WD repeat domain 19 | Immer | In 1 Erkrankung |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| BICC1BicC family RNA binding protein 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GANABglucosidase II alpha subunit | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NEK8NIMA related kinase 8 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PKD1polycystin 1, transient receptor potential channel interacting | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PKD2polycystin 2, transient receptor potential cation channel | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| UMODuromodulin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CCND1cyclin D1 | Häufig (30–79 %) | In 1 Erkrankung |
| DBHdopamine beta-hydroxylase | Häufig (30–79 %) | In 1 Erkrankung |
| HNF1BHNF1 homeobox B | Häufig (30–79 %) | In 1 Erkrankung |
| IFT56intraflagellar transport 56 | Häufig (30–79 %) | In 1 Erkrankung |
| MRPS7mitochondrial ribosomal protein S7 | Häufig (30–79 %) | In 1 Erkrankung |
| SLC22A12solute carrier family 22 member 12 | Häufig (30–79 %) | In 1 Erkrankung |
| TREX1three prime repair exonuclease 1 | Häufig (30–79 %) | In 1 Erkrankung |
| CTNScystinosin, lysosomal cystine transporter | Manchmal (5–29 %) | In 1 Erkrankung |
| HBBhemoglobin subunit beta | Manchmal (5–29 %) | In 1 Erkrankung |
| HPRT1hypoxanthine phosphoribosyltransferase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| NPHP1nephrocystin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Manchmal (5–29 %) | In 1 Erkrankung |
| CORINcorin, serine peptidase | Selten (1–4 %) | In 1 Erkrankung |
16 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| FLT1fms related receptor tyrosine kinase 1 | Selten (1–4 %) | In 1 Erkrankung |
| STOX1storkhead box 1 | Selten (1–4 %) | In 1 Erkrankung |
| ADAMTS13ADAM metallopeptidase with thrombospondin type 1 motif 13 | Nicht erfasst | In 1 Erkrankung |
| C3complement C3 | Nicht erfasst | In 1 Erkrankung |
| CD46CD46 molecule | Nicht erfasst | In 1 Erkrankung |
| CFBcomplement factor B | Nicht erfasst | In 1 Erkrankung |
| CFHcomplement factor H | Nicht erfasst | In 1 Erkrankung |
| CFHR1complement factor H related 1 | Nicht erfasst | In 1 Erkrankung |
| CFHR3complement factor H related 3 | Nicht erfasst | In 1 Erkrankung |
| CFIcomplement factor I | Nicht erfasst | In 1 Erkrankung |
| COQ7coenzyme Q7, hydroxylase | Nicht erfasst | In 1 Erkrankung |
| ELP1elongator acetyltransferase complex subunit 1 | Nicht erfasst | In 1 Erkrankung |
| FAN1FANCD2 and FANCI associated nuclease 1 | Nicht erfasst | In 1 Erkrankung |
| INVSinversin | Nicht erfasst | In 1 Erkrankung |
| MUC1mucin 1, cell surface associated | Nicht erfasst | In 1 Erkrankung |
| THBDthrombomodulin | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
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