Požymis
Extra ribs
Klinikinis pavadinimas: Supernumerary ribs
The presence of more than 12 rib pairs.
Santrauka
- Kūno sistema
- Abnormality of the musculoskeletal system
Ši puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/supernumerary-ribs.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Extra ribs, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test23 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.
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- MTX2-Related Mandibuloacral DysplasiaReads 1 of these genesMTX2About this report →
- X-linked Autoinflammatory DiseaseReads 1 of these genesIKBKGAbout this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesTBX6About this report →
Show 19 more reports
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesPTCH1About this report →
- Marfan Like SyndromesReads 2 of these genesTGFBR1SKIAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesNIPBLAbout this report →
- Hereditary SpherocytosisReads 1 of these genesANK1About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR1About this report →
- Waardenburg SyndromeReads 1 of these genesPAX3About this report →
- Aortic AneurysmReads 1 of these genesTGFBR1About this report →
- Diamond-Blackfan AnemiaReads 1 of these genesRPS26About this report →
- Ectodermal DysplasiasReads 1 of these genesIKBKGAbout this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesMAFAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesACTBAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesPTCH1About this report →
- VitreoretinopathyReads 1 of these genesIKBKGAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesSOX2About this report →
- Inherited ThrombocytopeniasReads 1 of these genesACTBAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesIKBKGAbout this report →
- Intellectual DisabilityReads 1 of these genesKDM6BAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Extra ribs, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test18 genų susiję su Extra ribs
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Extra ribs. Dauguma žmonių, turinčių šį požymį, neturi nė vienos iš tų ligų, o šiame sąraše esantis genas nieko nesako apie kieno nors paties genomą.
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| KDM6Blysine demethylase 6B | Visada | 1 ligoje |
| TGFBR1transforming growth factor beta receptor 1 | Visada | 1 ligoje |
| GDF11growth differentiation factor 11 | Labai dažnai (80–99%) | 1 ligoje |
| ACTBactin beta | Kartais (5–29%) | 1 ligoje |
| AFF3ALF transcription elongation factor 3 | Kartais (5–29%) | 1 ligoje |
| ANK1ankyrin 1 | Kartais (5–29%) | 1 ligoje |
| DOT1LDOT1 like histone lysine methyltransferase | Kartais (5–29%) | 1 ligoje |
| MAFMAF bZIP transcription factor | Kartais (5–29%) | 1 ligoje |
| MTX2metaxin 2 | Kartais (5–29%) | 1 ligoje |
| RPS26ribosomal protein S26 | Kartais (5–29%) | 1 ligoje |
| SKISKI proto-oncogene | Kartais (5–29%) | 1 ligoje |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Neužfiksuota | 1 ligoje |
| NIPBLNIPBL cohesin loading factor | Neužfiksuota | 1 ligoje |
| PAX3paired box 3 | Neužfiksuota | 1 ligoje |
| PTCH1patched 1 | Neužfiksuota | 1 ligoje |
| SIX6SIX homeobox 6 | Neužfiksuota | 1 ligoje |
| SOX2SRY-box transcription factor 2 | Neužfiksuota | 1 ligoje |
| TBX6T-box transcription factor 6 | Neužfiksuota | 1 ligoje |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Siauresni požymiai
Platesni požymiai
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.18-8b139e39.
From traits to your genome
Read the genes behind these traits in your own DNA.
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Nemokamas pristatymas · Rezultatai per 6–8 savaites
