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Træk
Birth weight > 90th percentile
Klinisk navn: Large for gestational age
The term large for gestational age applies to babies whose birth weight lies above the 90th percentile for that gestational age.
Resumé
- Også kaldet
- Birthweight > 90th percentile, Fetal macrosomia, Foetal macrosomia, Macrosomia, Macrosomia, neonatal
- Kropssystem
- Growth abnormality
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/large-for-gestational-age.json"
page <- fromJSON(url)
page$trait$nameBirth weight > 90th percentileHP:0001520
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Læs de gener, der er knyttet til Birth weight > 90th percentile, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test38 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.
- Maturity-Onset Diabetes Of The YoungReads 11 of these genesHNF4AABCC8HNF1AKCNJ11APPL1CELAbout this report →
- Diabetes MellitusReads 12 of these genesHNF4AAKT2ABCC8HNF1AKCNJ11APPL1About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesPTCH1SUFUAbout this report →
- Neonatal Diabetes MellitusReads 6 of these genesABCC8KCNJ11GCKINSNEUROD1PDX1About this report →
Show 34 more reports
- Noonan SyndromeReads 5 of these genesBRAFRIT1SHOC2SOS1RAF1About this report →
- DICER1 Tumour PredispositionReads 1 of these genesDICER1About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- PDX1-Related Pancreatic AgenesisReads 1 of these genesPDX1About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- HyperinsulinismReads 3 of these genesABCC8KCNJ11GCKAbout this report →
- GPI Anchor Biosynthesis DefectsReads 4 of these genesPIGAPIGLPIGNPIGTAbout this report →
- Hypertrophic CardiomyopathyReads 6 of these genesNSD1BRAFRIT1SHOC2SOS1RAF1About this report →
- Cantú SyndromeReads 1 of these genesABCC9About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Lung CancerReads 1 of these genesDICER1About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesAKT2About this report →
- Congenital MyopathiesReads 3 of these genesBIN1DNM2RYR1About this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesDLK1About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesMTORAbout this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGAPIGLPIGNPIGTAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 2 of these genesPTCH1GLI3About this report →
- Intellectual DisabilityReads 6 of these genesNDST1ANK3EHMT1KMT2CZFXPIGLAbout this report →
- Waardenburg SyndromeReads 1 of these genesEDNRBAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- LipodystrophyReads 1 of these genesAKT2About this report →
- Dilated CardiomyopathyReads 2 of these genesRAF1ABCC9About this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesIFT74About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZFXAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesDNM2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesPIGAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesDNM2About this report →
Læs de gener, der er knyttet til Birth weight > 90th percentile, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test54 gener knyttet til Birth weight > 90th percentile
Ændringer i disse gener forårsager sjældne tilstande, hvor Birth weight > 90th percentile ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| EDNRBendothelin receptor type B | Altid | I 1 tilstand |
| HERC1HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 | Altid | I 2 tilstande |
| HNF4Ahepatocyte nuclear factor 4 alpha | Altid | I 3 tilstande |
| IFT74intraflagellar transport 74 | Altid | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Altid | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Altid | I 1 tilstand |
| SPIN4spindlin family member 4 | Altid | I 1 tilstand |
| AKT2AKT serine/threonine kinase 2 | Meget ofte (80–99 %) | I 2 tilstande |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Meget ofte (80–99 %) | I 1 tilstand |
| PTCH1patched 1 | Meget ofte (80–99 %) | I 1 tilstand |
| RNF135ring finger protein 135 | Meget ofte (80–99 %) | I 1 tilstand |
| ABCC8ATP binding cassette subfamily C member 8 | Ofte (30–79 %) | I 3 tilstande |
| BIN1bridging integrator 1 | Ofte (30–79 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Ofte (30–79 %) | I 1 tilstand |
| DICER1dicer 1, ribonuclease III | Ofte (30–79 %) | I 1 tilstand |
| DLK1delta like non-canonical Notch ligand 1 | Ofte (30–79 %) | I 2 tilstande |
| DNM2dynamin 2 | Ofte (30–79 %) | I 1 tilstand |
| FIBPFGF1 intracellular binding protein | Ofte (30–79 %) | I 2 tilstande |
| HNF1AHNF1 homeobox A | Ofte (30–79 %) | I 2 tilstande |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Ofte (30–79 %) | I 4 tilstande |
| MEG3maternally expressed 3 | Ofte (30–79 %) | I 2 tilstande |
| MTMR14myotubularin related protein 14 | Ofte (30–79 %) | I 1 tilstand |
| MTORmechanistic target of rapamycin kinase | Ofte (30–79 %) | I 2 tilstande |
| MYF6myogenic factor 6 | Ofte (30–79 %) | I 1 tilstand |
| NDST1N-deacetylase and N-sulfotransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| ODC1ornithine decarboxylase 1 | Ofte (30–79 %) | I 2 tilstande |
| PTENphosphatase and tensin homolog | Ofte (30–79 %) | I 1 tilstand |
| RIT1Ras like without CAAX 1 | Ofte (30–79 %) | I 1 tilstand |
| RTL1retrotransposon Gag like 1 | Ofte (30–79 %) | I 2 tilstande |
| RYR1ryanodine receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Ofte (30–79 %) | I 1 tilstand |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Ofte (30–79 %) | I 1 tilstand |
| UCP2uncoupling protein 2 | Ofte (30–79 %) | I 1 tilstand |
| ANK3ankyrin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Nogle gange (5–29 %) | I 1 tilstand |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| CELcarboxyl ester lipase | Nogle gange (5–29 %) | I 1 tilstand |
| EHMT1euchromatic histone lysine methyltransferase 1 | Nogle gange (5–29 %) | I 2 tilstande |
| GCKglucokinase | Nogle gange (5–29 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Nogle gange (5–29 %) | I 1 tilstand |
Vis 14 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| INSinsulin | Nogle gange (5–29 %) | I 1 tilstand |
| KLF11KLF transcription factor 11 | Nogle gange (5–29 %) | I 1 tilstand |
| KMT2Clysine methyltransferase 2C | Nogle gange (5–29 %) | I 1 tilstand |
| NEUROD1neuronal differentiation 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PAX4paired box 4 | Nogle gange (5–29 %) | I 1 tilstand |
| PDX1pancreatic and duodenal homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| SUFUSUFU negative regulator of hedgehog signaling | Nogle gange (5–29 %) | I 1 tilstand |
| ZFXzinc finger protein X-linked | Nogle gange (5–29 %) | I 1 tilstand |
| ABCC9ATP binding cassette subfamily C member 9 | Ikke registreret | I 1 tilstand |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Ikke registreret | I 1 tilstand |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Ikke registreret | I 1 tilstand |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Ikke registreret | I 1 tilstand |
| TMCO1transmembrane and coiled-coil domains 1 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
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