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Egenskap
Decreased parathyroid hormone secretion
Klinisk navn: Hypoparathyroidism
A condition caused by a deficiency of parathyroid hormone characterized by hypocalcemia and hyperphosphatemia.
Sammendrag
- Også kalt
- Low parathyroid hormone
- Kroppssystem
- Abnormality of the endocrine system
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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/hypoparathyroidism.json"
page <- fromJSON(url)
page$trait$nameDecreased parathyroid hormone secretionHP:0000829
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Les genene knyttet til Decreased parathyroid hormone secretion, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test33 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.
- Alport SyndromeReads 3 of these genesCOL4A3COL4A4COL4A5About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Hereditary Optic NeuropathyReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
Show 29 more reports
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- FAM111A-Related Skeletal DysplasiaReads 1 of these genesFAM111AAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 2 of these genesGATA3PTHAbout this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 2 of these genesHADHAHADHBAbout this report →
- Leigh SyndromeReads 4 of these genesMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesHADHAMPV17RRM2BMT-ND1MT-ND4MT-ND5About this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- ThalassaemiaReads 1 of these genesHBBAbout this report →
- Thyroid CancerReads 2 of these genesPTHAIREAbout this report →
- PolycythemiaReads 1 of these genesHBBAbout this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Inherited Neurodegenerative DisordersReads 5 of these genesTBCEMT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGTAbout this report →
- Autoimmune DiseaseReads 1 of these genesAIREAbout this report →
- Diabetes MellitusReads 1 of these genesMT-TL1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGP1BBAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesMPV17RRM2BAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesCHD7About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesHADHAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesMPV17About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPIGTAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTBX1About this report →
- Intellectual DisabilityReads 1 of these genesJMJD1CAbout this report →
Les genene knyttet til Decreased parathyroid hormone secretion, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test50 gener knyttet til Decreased parathyroid hormone secretion
Endringer i disse genene forårsaker sjeldne tilstander der Decreased parathyroid hormone secretion 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 |
|---|---|---|
| GATA3GATA binding protein 3 | Alltid | I 2 tilstander |
| KDM6Alysine demethylase 6A | Alltid | I 1 tilstand |
| KMT2Dlysine methyltransferase 2D | Alltid | I 1 tilstand |
| PTHparathyroid hormone | Alltid | I 1 tilstand |
| AIREautoimmune regulator | Svært ofte (80–99 %) | I 2 tilstander |
| TBCEtubulin folding cofactor E | Svært ofte (80–99 %) | I 2 tilstander |
| ARVCFARVCF delta catenin family member | Ofte (30–79 %) | I 1 tilstand |
| CHD7chromodomain helicase DNA binding protein 7 | Ofte (30–79 %) | I 1 tilstand |
| COMTcatechol-O-methyltransferase | Ofte (30–79 %) | I 1 tilstand |
| GP1BBglycoprotein Ib platelet subunit beta | Ofte (30–79 %) | I 1 tilstand |
| HIRAhistone cell cycle regulator | Ofte (30–79 %) | I 1 tilstand |
| IRX5iroquois homeobox 5 | Ofte (30–79 %) | I 1 tilstand |
| JMJD1Cjumonji domain containing 1C | Ofte (30–79 %) | I 1 tilstand |
| RREB1ras responsive element binding protein 1 | Ofte (30–79 %) | I 1 tilstand |
| SEC24CSEC24 homolog C, COPII component | Ofte (30–79 %) | I 1 tilstand |
| TBX1T-box transcription factor 1 | Ofte (30–79 %) | I 2 tilstander |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Ofte (30–79 %) | I 1 tilstand |
| ATP7BATPase copper transporting beta | Noen ganger (5–29 %) | I 2 tilstander |
| DGCR2DiGeorge syndrome critical region gene 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DGCR6DiGeorge syndrome critical region gene 6 | Noen ganger (5–29 %) | I 1 tilstand |
| DGCR8DGCR8 microprocessor complex subunit | Noen ganger (5–29 %) | I 1 tilstand |
| ESS2ess-2 spliceosome associated protein | Noen ganger (5–29 %) | I 1 tilstand |
| HADHAhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| HBBhemoglobin subunit beta | Noen ganger (5–29 %) | I 3 tilstander |
| MPV17mitochondrial inner membrane protein MPV17 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Noen ganger (5–29 %) | I 2 tilstander |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Noen ganger (5–29 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Noen ganger (5–29 %) | I 1 tilstand |
| TBX2T-box transcription factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Sjelden (1–4%) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Sjelden (1–4%) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Sjelden (1–4%) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Sjelden (1–4%) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Sjelden (1–4%) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Sjelden (1–4%) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Sjelden (1–4%) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Sjelden (1–4%) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Sjelden (1–4%) | I 1 tilstand |
Vis 10 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Sjelden (1–4%) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Sjelden (1–4%) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Sjelden (1–4%) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Sjelden (1–4%) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Sjelden (1–4%) | I 1 tilstand |
| COL4A3collagen type IV alpha 3 chain | Ikke registrert | I 1 tilstand |
| COL4A4collagen type IV alpha 4 chain | Ikke registrert | I 1 tilstand |
| COL4A5collagen type IV alpha 5 chain | Ikke registrert | I 1 tilstand |
| FAM111AFAM111 trypsin like peptidase A | Ikke registrert | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | 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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