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Egenskap
Increased body weight
Abnormally increased body weight.
Sammendrag
- Også kalt
- Weight gain
- Kroppssystem
- Growth 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/increased-body-weight.json"
page <- fromJSON(url)
page$trait$nameIncreased body weightHP:0004324
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Les genene knyttet til Increased body weight, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test44 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.
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 3 of these genesPRKAR1AARMC5PDE11AAbout this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 3 of these genesCD46CFHCFIAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesPRKAR1AGNASAbout this report →
- Chung-Jansen Syndrome (PHIP)Reads 1 of these genesPHIPAbout this report →
Show 40 more reports
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Glycogen Storage DiseaseReads 3 of these genesPHKA2PHKBPHKG2About this report →
- Thyroid CancerReads 4 of these genesTHRBMEN1GNASTHRAAbout this report →
- Malignant Endocrine NeoplasmReads 2 of these genesMEN1TP53About this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesNSD1MAGEL2About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- HyperthyroidismReads 1 of these genesTHRBAbout this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesTHRBAbout this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF4AAbout this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- Intellectual DisabilityReads 4 of these genesATRXCTNNB1RAI1UBE2AAbout this report →
- Hypertrophic CardiomyopathyReads 2 of these genesNSD1BRAFAbout this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesCFIAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Epidermolysis BullosaReads 1 of these genesDSTAbout this report →
- Congenital HypothyroidismReads 1 of these genesTHRAAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesDSTAbout this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesCD46CFHCFIAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23USP48About this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Diabetes MellitusReads 1 of these genesHNF4AAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesMAGEL2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesDSTFDXRAbout this report →
- Epilepsy (Full Panel)Reads 1 of these genesRNU2-2About this report →
Les genene knyttet til Increased body weight, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test40 gener knyttet til Increased body weight
Endringer i disse genene forårsaker sjeldne tilstander der Increased body weight 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 |
|---|---|---|
| CHASERRCHD2 adjacent suppressive regulatory RNA | Alltid | I 1 tilstand |
| DSTdystonin | Alltid | I 1 tilstand |
| FDXRferredoxin reductase | Alltid | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Alltid | I 1 tilstand |
| RNU2-2RNA, U2 small nuclear 2 | Alltid | I 1 tilstand |
| THRBthyroid hormone receptor beta | Alltid | I 1 tilstand |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Alltid | I 1 tilstand |
| ATP7BATPase copper transporting beta | Svært ofte (80–99 %) | I 1 tilstand |
| HNF4Ahepatocyte nuclear factor 4 alpha | Svært ofte (80–99 %) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Ofte (30–79 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Ofte (30–79 %) | I 1 tilstand |
| CD46CD46 molecule | Ofte (30–79 %) | I 1 tilstand |
| CDH23cadherin related 23 | Ofte (30–79 %) | I 1 tilstand |
| CDKN2Acyclin dependent kinase inhibitor 2A | Ofte (30–79 %) | I 1 tilstand |
| CFHcomplement factor H | Ofte (30–79 %) | I 1 tilstand |
| CFIcomplement factor I | Ofte (30–79 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Ofte (30–79 %) | I 1 tilstand |
| HELLPARHELLP associated long non-coding RNA | Ofte (30–79 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Ofte (30–79 %) | I 1 tilstand |
| MEN1menin 1 | Ofte (30–79 %) | I 1 tilstand |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Ofte (30–79 %) | I 1 tilstand |
| PHIPPHIP subunit of CUL4-Ring ligase complex | Ofte (30–79 %) | I 1 tilstand |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Ofte (30–79 %) | I 2 tilstander |
| RAI1retinoic acid induced 1 | Ofte (30–79 %) | I 1 tilstand |
| TERTtelomerase reverse transcriptase | Ofte (30–79 %) | I 1 tilstand |
| TP53tumor protein p53 | Ofte (30–79 %) | I 2 tilstander |
| USP48ubiquitin specific peptidase 48 | Ofte (30–79 %) | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | Ofte (30–79 %) | I 1 tilstand |
| YY1YY1 transcription factor | Ofte (30–79 %) | I 1 tilstand |
| ZNRF3zinc and ring finger 3 | Ofte (30–79 %) | I 1 tilstand |
| ARMC5armadillo repeat containing 5 | Noen ganger (5–29 %) | I 2 tilstander |
| GNASGNAS complex locus | Noen ganger (5–29 %) | I 1 tilstand |
| KDM1Alysine demethylase 1A | Noen ganger (5–29 %) | I 1 tilstand |
| PDE11Aphosphodiesterase 11A | Noen ganger (5–29 %) | I 1 tilstand |
| UBE2Aubiquitin conjugating enzyme E2 A | Noen ganger (5–29 %) | I 1 tilstand |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Sjelden (1–4%) | I 1 tilstand |
| PHKBphosphorylase kinase regulatory subunit beta | Sjelden (1–4%) | I 1 tilstand |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Sjelden (1–4%) | I 1 tilstand |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Ikke registrert | I 1 tilstand |
| THRAthyroid hormone receptor alpha | 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.
Smalere egenskaper
Bredere egenskaper
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.
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
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Read the genes behind these traits in your own DNA.
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