AtlasPožymis
Leg paralysis
Klinikinis pavadinimas: Paraplegia
Severe or complete weakness of both lower extremities with sparing of the upper extremities.
Santrauka
- Kūno sistema
- Abnormality of the nervous system
AtlasŠi puslapis kaip duomenys
Norėdami perskaityti jį kaip JSON, pridėkite .json prie puslapio adreso arba nurodykite application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/paraplegia.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Leg paralysis, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test21 condition report reads 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.
- Hypogonadotropic HypogonadismReads 13 of these genesANOS1CHD7FEZF1FGF17FGF8FGFR1About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- DCC-Related Mirror Movements and Agenesis of the Corpus CallosumReads 1 of these genesDCCAbout this report →
- Hepatic Veno-Occlusive Disease with Immunodeficiency (VODI)Reads 1 of these genesSP110About this report →
Show 17 more reports
- L1 SyndromeReads 1 of these genesL1CAMAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesRASA1About this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesSAMD9About this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesATL1L1CAMSPASTZFYVE26About this report →
- Distal MyopathiesReads 2 of these genesGIPC1LRP12About this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Hereditary AmyloidosisReads 1 of these genesTTRAbout this report →
- Urea Cycle DisorderReads 1 of these genesNAGSAbout this report →
- Ehlers-Danlos SyndromeReads 1 of these genesB3GALT6About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesATL1About this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Inherited Neurodegenerative DisordersReads 4 of these genesATL1L1CAMSPASTZFYVE26About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesHESX1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesATL1TTRAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesB3GALT6About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSP110About this report →
- Intellectual DisabilityReads 1 of these genesWDR11About this report →
Vienu tyrimu sužinokite genus, susijusius su Leg paralysis, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test42 genų susiję su Leg paralysis
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Leg paralysis. 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 |
|---|---|---|
| EEFSECeukaryotic elongation factor, selenocysteine-tRNA specific | Visada | 1 ligoje |
| ELFN1extracellular leucine rich repeat and fibronectin type III domain containing 1 | Visada | 1 ligoje |
| NFU1NFU1 iron-sulfur cluster scaffold | Visada | 1 ligoje |
| CKAP2Lcytoskeleton associated protein 2L | Dažnai (30–79%) | 1 ligoje |
| ANOS1anosmin 1 | Kartais (5–29%) | 1 ligoje |
| CCDC141coiled-coil domain containing 141 | Kartais (5–29%) | 1 ligoje |
| CHD7chromodomain helicase DNA binding protein 7 | Kartais (5–29%) | 1 ligoje |
| DCCDCC netrin 1 receptor | Kartais (5–29%) | 1 ligoje |
| DUSP6dual specificity phosphatase 6 | Kartais (5–29%) | 1 ligoje |
| EMX2empty spiracles homeobox 2 | Kartais (5–29%) | 1 ligoje |
| FEZF1FEZ family zinc finger 1 | Kartais (5–29%) | 1 ligoje |
| FGF17fibroblast growth factor 17 | Kartais (5–29%) | 1 ligoje |
| FGF8fibroblast growth factor 8 | Kartais (5–29%) | 1 ligoje |
| FGFR1fibroblast growth factor receptor 1 | Kartais (5–29%) | 1 ligoje |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Kartais (5–29%) | 1 ligoje |
| HESX1HESX homeobox 1 | Kartais (5–29%) | 1 ligoje |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Kartais (5–29%) | 1 ligoje |
| IL17RDinterleukin 17 receptor D | Kartais (5–29%) | 1 ligoje |
| NDNFneuron derived neurotrophic factor | Kartais (5–29%) | 1 ligoje |
| PROK2prokineticin 2 | Kartais (5–29%) | 1 ligoje |
| PROKR2prokineticin receptor 2 | Kartais (5–29%) | 1 ligoje |
| SAMD9sterile alpha motif domain containing 9 | Kartais (5–29%) | 1 ligoje |
| SEMA3Asemaphorin 3A | Kartais (5–29%) | 1 ligoje |
| SOX10SRY-box transcription factor 10 | Kartais (5–29%) | 1 ligoje |
| SP110SP110 nuclear body protein | Kartais (5–29%) | 1 ligoje |
| SPRY4sprouty RTK signaling antagonist 4 | Kartais (5–29%) | 1 ligoje |
| TACR3tachykinin receptor 3 | Kartais (5–29%) | 1 ligoje |
| WDR11WD repeat domain 11 | Kartais (5–29%) | 1 ligoje |
| ABCD3ATP binding cassette subfamily D member 3 | Retai (1–4 %) | 1 ligoje |
| GIPC1GIPC PDZ domain containing family member 1 | Retai (1–4 %) | 1 ligoje |
| LRP12LDL receptor related protein 12 | Retai (1–4 %) | 1 ligoje |
| NAGSN-acetylglutamate synthase | Retai (1–4 %) | 1 ligoje |
| NOTCH2NLCnotch 2 N-terminal like C | Retai (1–4 %) | 1 ligoje |
| NUTM2B-AS1NUTM2B antisense RNA 1 | Retai (1–4 %) | 1 ligoje |
| RASA1RAS p21 protein activator 1 | Retai (1–4 %) | 1 ligoje |
| RILPL1Rab interacting lysosomal protein like 1 | Retai (1–4 %) | 1 ligoje |
| ATL1atlastin GTPase 1 | Neužfiksuota | 1 ligoje |
| B3GALT6beta-1,3-galactosyltransferase 6 | Neužfiksuota | 1 ligoje |
| L1CAML1 cell adhesion molecule | Neužfiksuota | 1 ligoje |
| SPASTspastin | Neužfiksuota | 1 ligoje |
Rodyti dar 2 genų
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
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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 2026.10.19-9814e911.
AtlasFrom traits to your genome
Read the genes behind these traits in your own DNA.
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