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Egenskap
Low blood phosphate level
Klinisk navn: Hypophosphatemia
The concentration of phosphate ion in the blood circulation is below the lower limit of normal.
Sammendrag
- Også kalt
- Decreased phosphate ion concentration, Decreased phosphate ion level, Decreased phosphate ion level in blood, Hypophosphataemia, Reduced phosphate ion concentration, Reduced phosphate ion level, Reduced phosphate ion level in blood
- Kroppssystem
- Laboratory abnormality
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypophosphatemia.json"
page <- fromJSON(url)
page$trait$nameLow blood phosphate levelHP:0002148
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Les genene knyttet til Low blood phosphate level, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test31 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.
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 7 of these genesCYP27B1CYP2R1PHEXSLC34A3FGF23VDRAbout this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 4 of these genesCDC73GCM2AP2S1CASRAbout this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 3 of these genesHNF4AEHHADHGATMAbout this report →
- Dent Disease and Lowe SyndromeReads 2 of these genesOCRLCLCN5About this report →
Show 27 more reports
- OsteopetrosisReads 5 of these genesCLCN7OSTM1SNX10TCIRG1TNFSF11About this report →
- CLCN7-Related Hypopigmentation, Organomegaly and Delayed Myelination (HOD)Reads 1 of these genesCLCN7About this report →
- CystinosisReads 1 of these genesCTNSAbout this report →
- OpsismodysplasiaReads 1 of these genesINPPL1About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Raine SyndromeReads 1 of these genesFAM20CAbout this report →
- Thyroid CancerReads 5 of these genesCDC73GCM2MEN1GNASCASRAbout this report →
- Malignant Endocrine NeoplasmReads 2 of these genesCDC73MEN1About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hypercalcemia InfantileReads 1 of these genesSLC34A1About this report →
- Inherited ArthropathiesReads 1 of these genesANKHAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesCACNA1SAbout this report →
- Alport SyndromeReads 1 of these genesCOL4A3About this report →
- Cerebral Creatine Deficiency SyndromesReads 1 of these genesGATMAbout this report →
- Familial Periodic ParalysisReads 1 of these genesCACNA1SAbout this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesALDOBAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Diabetes MellitusReads 2 of these genesHNF4ASLC2A2About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF4AAbout this report →
- Glycogen Storage DiseaseReads 1 of these genesSLC2A2About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesHMGCS2About this report →
- Neonatal Diabetes MellitusReads 1 of these genesSLC2A2About this report →
- Primary Mitochondrial DiseaseReads 2 of these genesNDUFAF6POLRMTAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesCTNSAbout this report →
- Leigh SyndromeReads 1 of these genesNDUFAF6About this report →
- Epilepsy (Full Panel)Reads 1 of these genesGABRA3About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesNDUFAF6About this report →
Les genene knyttet til Low blood phosphate level, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test41 gener knyttet til Low blood phosphate level
Endringer i disse genene forårsaker sjeldne tilstander der Low blood phosphate level forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| CTNScystinosin, lysosomal cystine transporter | Alltid | I 3 tilstander |
| CYP27B1cytochrome P450 family 27 subfamily B member 1 | Alltid | I 2 tilstander |
| CYP2R1cytochrome P450 family 2 subfamily R member 1 | Alltid | I 2 tilstander |
| HMGCS23-hydroxy-3-methylglutaryl-CoA synthase 2 | Alltid | I 1 tilstand |
| HNF4Ahepatocyte nuclear factor 4 alpha | Alltid | I 1 tilstand |
| PHEXphosphate regulating endopeptidase X-linked | Alltid | I 2 tilstander |
| SLC34A1solute carrier family 34 member 1 | Alltid | I 5 tilstander |
| SLC34A3solute carrier family 34 member 3 | Alltid | I 2 tilstander |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Svært ofte (80–99 %) | I 1 tilstand |
| CDC73cell division cycle 73 | Svært ofte (80–99 %) | I 3 tilstander |
| FGF23fibroblast growth factor 23 | Svært ofte (80–99 %) | I 2 tilstander |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Svært ofte (80–99 %) | I 1 tilstand |
| GCM2GCM transcription factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| INPPL1inositol polyphosphate phosphatase like 1 | Svært ofte (80–99 %) | I 1 tilstand |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Svært ofte (80–99 %) | I 1 tilstand |
| MEN1menin 1 | Svært ofte (80–99 %) | I 1 tilstand |
| SLC2A2solute carrier family 2 member 2 | Svært ofte (80–99 %) | I 2 tilstander |
| VDRvitamin D receptor | Svært ofte (80–99 %) | I 2 tilstander |
| ANKHANKH inorganic pyrophosphate transport regulator | Ofte (30–79 %) | I 1 tilstand |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| GATMglycine amidinotransferase | Ofte (30–79 %) | I 2 tilstander |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Ofte (30–79 %) | I 2 tilstander |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Ofte (30–79 %) | I 2 tilstander |
| PTH1Rparathyroid hormone 1 receptor | Ofte (30–79 %) | I 2 tilstander |
| ALDOBaldolase, fructose-bisphosphate B | Noen ganger (5–29 %) | I 2 tilstander |
| CLCN7Cl-/H+ antiporter 7 | Noen ganger (5–29 %) | I 1 tilstand |
| FBXO22F-box protein 22 | Noen ganger (5–29 %) | I 1 tilstand |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| POLRMTRNA polymerase mitochondrial | Noen ganger (5–29 %) | I 1 tilstand |
| SNX10sorting nexin 10 | Noen ganger (5–29 %) | I 1 tilstand |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Noen ganger (5–29 %) | I 1 tilstand |
| TNFSF11TNF superfamily member 11 | Noen ganger (5–29 %) | I 1 tilstand |
| GNASGNAS complex locus | Sjelden (1–4%) | I 1 tilstand |
| AP2S1adaptor related protein complex 2 subunit sigma 1 | Ikke registrert | I 1 tilstand |
| CASRcalcium sensing receptor | Ikke registrert | I 1 tilstand |
| CLCN5Cl-/H+ antiporter 5 | Ikke registrert | I 3 tilstander |
| COL4A3collagen type IV alpha 3 chain | Ikke registrert | I 1 tilstand |
| CYP3A4cytochrome P450 family 3 subfamily A member 4 | Ikke registrert | I 1 tilstand |
| DMP1dentin matrix acidic phosphoprotein 1 | Ikke registrert | I 1 tilstand |
| FAM20CFAM20C golgi associated secretory pathway kinase | Ikke registrert | I 1 tilstand |
Vis 1 gen til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| NHERF1NHERF family PDZ scaffold protein 1 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.19-9814e911.
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