AtlasEgenskap
Abnormal endocardium morphology
An abnormality of the endocardium.
Sammendrag
- Også kalt
- Abnormality of the endocardium, Abnormality of the endomycoardium
- Kroppssystem
- Abnormality of the cardiovascular system
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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/abnormal-endocardium-morphology.json"
page <- fromJSON(url)
page$trait$nameLes genene knyttet til Abnormal endocardium morphology, og resten av genomet ditt, med én test.
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Få mitt Genome Test19 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.
- Chronic Mucocutaneous CandidiasisReads 3 of these genesIL17RAIL17RCTRAF3IP2About this report →
- Hereditary Arterial CalcificationReads 2 of these genesABCC6ENPP1About this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Pseudoxanthoma ElasticumReads 1 of these genesABCC6About this report →
Show 15 more reports
- Noonan SyndromeReads 3 of these genesBRAFPTPN11RAF1About this report →
- Hypertrophic CardiomyopathyReads 4 of these genesBRAFMYH7PTPN11RAF1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Left Ventricular NoncompactionReads 1 of these genesMYH7About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12BAbout this report →
- Dilated CardiomyopathyReads 2 of these genesMYH7RAF1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Other Inborn Errors of ImmunityReads 4 of these genesIL17RAIL17RCNCF1TRAF3IP2About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Distal MyopathiesReads 1 of these genesMYH7About this report →
- Congenital MyopathiesReads 1 of these genesMYH7About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGLAAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
Les genene knyttet til Abnormal endocardium morphology, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test33 gener knyttet til Abnormal endocardium morphology
Endringer i disse genene forårsaker sjeldne tilstander der Abnormal endocardium morphology 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 |
|---|---|---|
| ABCC6ATP binding cassette subfamily C member 6 | Noen ganger (5–29 %) | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Noen ganger (5–29 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Noen ganger (5–29 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Noen ganger (5–29 %) | I 1 tilstand |
| CLEC7AC-type lectin domain containing 7A | Noen ganger (5–29 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Noen ganger (5–29 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Noen ganger (5–29 %) | I 1 tilstand |
| ELNelastin | Noen ganger (5–29 %) | I 1 tilstand |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Noen ganger (5–29 %) | I 1 tilstand |
| GLAgalactosidase alpha | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2Igeneral transcription factor IIi | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Noen ganger (5–29 %) | I 1 tilstand |
| IL12Binterleukin 12B | Noen ganger (5–29 %) | I 1 tilstand |
| IL17Finterleukin 17F | Noen ganger (5–29 %) | I 1 tilstand |
| IL17RAinterleukin 17 receptor A | Noen ganger (5–29 %) | I 1 tilstand |
| IL17RCinterleukin 17 receptor C | Noen ganger (5–29 %) | I 1 tilstand |
| LIMK1LIM domain kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Noen ganger (5–29 %) | I 1 tilstand |
| MLXMAX dimerization protein MLX | Noen ganger (5–29 %) | I 1 tilstand |
| MYH7myosin heavy chain 7 | Noen ganger (5–29 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Noen ganger (5–29 %) | I 1 tilstand |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Noen ganger (5–29 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Noen ganger (5–29 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Noen ganger (5–29 %) | I 1 tilstand |
| TRAF3IP2TRAF3 interacting protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Noen ganger (5–29 %) | 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 2026.10.21-777c9289.
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