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Træk
Abnormally shaped kidney
Klinisk navn: Abnormal renal morphology
Any structural anomaly of the kidney.
Resumé
- Også kaldet
- Kidney malformation, Kidney structure issue, Structural kidney abnormalities, Abnormal kidney morphology, Renal malformation, Structural anomalies of the renal tract, Structural renal anomalies
- Kropssystem
- Abnormality of the genitourinary system
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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/abnormal-renal-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormally shaped kidneyHP:0012210
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Læs de gener, der er knyttet til Abnormally shaped kidney, og resten af dit genom, med én test.
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Bestil min Genome Test29 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.
- Fanconi AnemiaReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- DNA Repair DiseaseReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
Show 25 more reports
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Phenylketonuria (PKU)Reads 1 of these genesPAHAbout this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- Hereditary Vascular MalformationsReads 1 of these genesGLMNAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR2PORAbout this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesPORAbout this report →
- Kidney CancerReads 1 of these genesFLCNAbout this report →
- Male InfertilityReads 2 of these genesFANCMCFTRAbout this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF1BAbout this report →
- Urinary and Renal System TumourReads 1 of these genesFLCNAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGVAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Congenital Disorders of GlycosylationReads 2 of these genesSLC35A2PIGVAbout this report →
- Diabetes MellitusReads 1 of these genesHNF1BAbout this report →
- Female InfertilityReads 1 of these genesFANCMAbout this report →
- Intellectual DisabilityReads 2 of these genesRAI1PACS1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesSLC35A2About this report →
Læs de gener, der er knyttet til Abnormally shaped kidney, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test40 gener knyttet til Abnormally shaped kidney
Ændringer i disse gener forårsager sjældne tilstande, hvor Abnormally shaped kidney 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 |
|---|---|---|
| BRCA1BRCA1 DNA repair associated | Ofte (30–79 %) | I 1 tilstand |
| BRCA2BRCA2 DNA repair associated | Ofte (30–79 %) | I 1 tilstand |
| BRIP1BRCA1 interacting DNA helicase 1 | Ofte (30–79 %) | I 1 tilstand |
| ELNelastin | Ofte (30–79 %) | I 1 tilstand |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| FAAP100FA core complex associated protein 100 | Ofte (30–79 %) | I 1 tilstand |
| FANCAFA complementation group A | Ofte (30–79 %) | I 2 tilstande |
| FANCBFA complementation group B | Ofte (30–79 %) | I 1 tilstand |
| FANCCFA complementation group C | Ofte (30–79 %) | I 1 tilstand |
| FANCD2FA complementation group D2 | Ofte (30–79 %) | I 1 tilstand |
| FANCEFA complementation group E | Ofte (30–79 %) | I 1 tilstand |
| FANCFFA complementation group F | Ofte (30–79 %) | I 1 tilstand |
| FANCGFA complementation group G | Ofte (30–79 %) | I 1 tilstand |
| FANCIFA complementation group I | Ofte (30–79 %) | I 2 tilstande |
| FANCLFA complementation group L | Ofte (30–79 %) | I 1 tilstand |
| FANCMFA complementation group M | Ofte (30–79 %) | I 1 tilstand |
| MAD2L2mitotic arrest deficient 2 like 2 | Ofte (30–79 %) | I 1 tilstand |
| MLXIPLMLX interacting protein like | Ofte (30–79 %) | I 1 tilstand |
| PALB2partner and localizer of BRCA2 | Ofte (30–79 %) | I 1 tilstand |
| RAD51RAD51 recombinase | Ofte (30–79 %) | I 1 tilstand |
| RAD51CRAD51 paralog C | Ofte (30–79 %) | I 1 tilstand |
| RAI1retinoic acid induced 1 | Ofte (30–79 %) | I 3 tilstande |
| RFWD3ring finger and WD repeat domain 3 | Ofte (30–79 %) | I 1 tilstand |
| SLX4SLX4 structure-specific endonuclease subunit | Ofte (30–79 %) | I 1 tilstand |
| UBE2Tubiquitin conjugating enzyme E2 T | Ofte (30–79 %) | I 1 tilstand |
| XRCC2X-ray repair cross complementing 2 | Ofte (30–79 %) | I 1 tilstand |
| ADGRG2adhesion G protein-coupled receptor G2 | Nogle gange (5–29 %) | I 1 tilstand |
| CFTRCF transmembrane conductance regulator | Nogle gange (5–29 %) | I 1 tilstand |
| DACT1dishevelled binding antagonist of beta catenin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HNF1BHNF1 homeobox B | Nogle gange (5–29 %) | I 1 tilstand |
| NF1neurofibromin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PACS1phosphofurin acidic cluster sorting protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SALL1spalt like transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GLMNglomulin, FKBP associated protein | Sjældent (1–4%) | I 1 tilstand |
| PAHphenylalanine hydroxylase | Sjældent (1–4%) | I 1 tilstand |
| SLC35A2solute carrier family 35 member A2 | Sjældent (1–4%) | I 1 tilstand |
| FGFR2fibroblast growth factor receptor 2 | Ikke registreret | I 1 tilstand |
| FLCNfolliculin | Ikke registreret | I 1 tilstand |
| PIGVphosphatidylinositol glycan anchor biosynthesis class V | Ikke registreret | I 1 tilstand |
| PORcytochrome p450 oxidoreductase | 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.
Snævrere træk
- Kidney stone132 gener
- Cystic kidney disease129 gener
- Increased calcium level in kidney97 gener
- Renal dysplasia75 gener
- Absent/small kidney73 gener
- Enlarged kidney48 gener
- Abnormal localisation of kidneys40 gener
- Extra kidney36 gener
- Fatty kidney11 gener
- Renal amyloidosis10 gener
- Abnormal rotation of the kidneys8 gener
- Abnormal renal collecting system morphology6 gener
- Kidney degeneration5 gener
- Abnormal renal interstitial morphology2 gener
- Abnormal renal medulla morphology2 gener
- Nephrogenic rest2 gener
- Renal fibrosis2 gener
- Abnormal renal cortex morphology1 gen
- Scarring of kidney arteries1 gen
- Abnormal nephron morphology
- Abnormal renal calyx morphology
- Abnormal renal echogenicity
- Abnormal renal pelvis morphology
- Abnormal renal vascular morphology
- Renal necrosis
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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