Požymis
Spastic diplegia
Spasticity (neuromuscular hypertonia) primarily in the muscles of the legs, hips, and pelvis.
Santrauka
- Taip pat vadinama
- Spastic diparesis, Spastic diplegic
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page$trait$nameVienu tyrimu sužinokite genus, susijusius su Spastic diplegia, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test54 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.
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- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- HSD10 Mitochondrial DiseaseReads 1 of these genesHSD17B10About this report →
- HyperlysinaemiaReads 1 of these genesAASSAbout this report →
Show 50 more reports
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
- Purine Nucleoside Phosphorylase DeficiencyReads 1 of these genesPNPAbout this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Inherited Neurodegenerative DisordersReads 18 of these genesALDH3A2AARS1ALS2ATP13A2DARS1ERLIN1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 4 of these genesRAB3GAP1RAB3GAP2BCORSOX2About this report →
- Metachromatic LeukodystrophyReads 1 of these genesPSAPAbout this report →
- Other Inherited LeukodystrophiesReads 6 of these genesALDH3A2AARS1DARS1GALCRNU7-1PSAPAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 2 of these genesELP2ADD3About this report →
- Rare Hereditary Peripheral NeuropathiesReads 10 of these genesAARS1GALCPDHXSIGMAR1SORDSPG11About this report →
- Lissencephaly Spectrum DisordersReads 3 of these genesRAB3GAP1RAB3GAP2NDE1About this report →
- TubulinopathiesReads 1 of these genesTUBB3About this report →
- Intellectual DisabilityReads 7 of these genesELP2AP1S2PQBP1TAF1CTNNB1HUWE1About this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesAARS1SIGMAR1SORDSPG11About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesSPTLC1SPTLC2About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesAP1S2RNU4-2About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesHSD17B4About this report →
- Lysosomal Storage DiseaseReads 3 of these genesGALCGNEPSAPAbout this report →
- Classic Organic AciduriasReads 1 of these genesGCDHAbout this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesTUBB3About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesATP13A2ERLIN1SPG11About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesRNU7-1About this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesGLRX5About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesRNU7-1ACP5About this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesPDHXAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesATP13A2About this report →
- Type I InterferonopathiesReads 1 of these genesACP5About this report →
- Urea Cycle DisorderReads 1 of these genesSLC25A15About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesATP13A2About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBB3About this report →
- Parkinson DiseaseReads 1 of these genesATP13A2About this report →
- Distal MyopathiesReads 1 of these genesGNEAbout this report →
- Epilepsy (Full Panel)Reads 3 of these genesAARS1FLNANTRK2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesDARS1About this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Spinal Muscular AtrophyReads 1 of these genesSIGMAR1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesGNEAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesTAF1About this report →
- Dilated CardiomyopathyReads 1 of these genesSYNE1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesRAB3GAP2About this report →
- Female InfertilityReads 1 of these genesHSD17B4About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSYNE1About this report →
- Leigh SyndromeReads 1 of these genesPDHXAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesGNEAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesCOXFA4About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRNU7-1About this report →
Vienu tyrimu sužinokite genus, susijusius su Spastic diplegia, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test57 genų susiję su Spastic diplegia
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Spastic diplegia. 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 |
|---|---|---|
| CFAP20cilia and flagella associated protein 20 | Visada | 1 ligoje |
| ELP2elongator acetyltransferase complex subunit 2 | Visada | 1 ligoje |
| LRRC7leucine rich repeat containing 7 | Visada | 1 ligoje |
| MSL2MSL complex subunit 2 | Visada | 1 ligoje |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Visada | 2 ligose |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Visada | 2 ligose |
| UNC13Aunc-13 homolog A | Visada | 1 ligoje |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Labai dažnai (80–99%) | 1 ligoje |
| AP1S2adaptor related protein complex 1 subunit sigma 2 | Labai dažnai (80–99%) | 1 ligoje |
| AARS1alanyl-tRNA synthetase 1 | Dažnai (30–79%) | 1 ligoje |
| ALS2alsin Rho guanine nucleotide exchange factor ALS2 | Dažnai (30–79%) | 2 ligose |
| ATP13A2ATPase cation transporting 13A2 | Dažnai (30–79%) | 1 ligoje |
| DARS1aspartyl-tRNA synthetase 1 | Dažnai (30–79%) | 1 ligoje |
| ERLIN1ER lipid raft associated 1 | Dažnai (30–79%) | 1 ligoje |
| FUSFUS RNA binding protein | Dažnai (30–79%) | 1 ligoje |
| GALCgalactosylceramidase | Dažnai (30–79%) | 2 ligose |
| GLRX5glutaredoxin 5 | Dažnai (30–79%) | 2 ligose |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Dažnai (30–79%) | 1 ligoje |
| NDE1nudE neurodevelopment protein 1 | Dažnai (30–79%) | 1 ligoje |
| PDHXpyruvate dehydrogenase complex component X | Dažnai (30–79%) | 1 ligoje |
| PQBP1polyglutamine binding protein 1 | Dažnai (30–79%) | 1 ligoje |
| SIGMAR1sigma receptor chaperone 1 | Dažnai (30–79%) | 1 ligoje |
| SLC25A15solute carrier family 25 member 15 | Dažnai (30–79%) | 1 ligoje |
| SORDsorbitol dehydrogenase | Dažnai (30–79%) | 1 ligoje |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Dažnai (30–79%) | 1 ligoje |
| SPTLC1serine palmitoyltransferase long chain base subunit 1 | Dažnai (30–79%) | 1 ligoje |
| SPTLC2serine palmitoyltransferase long chain base subunit 2 | Dažnai (30–79%) | 1 ligoje |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Dažnai (30–79%) | 1 ligoje |
| TAF1TATA-box binding protein associated factor 1 | Dažnai (30–79%) | 2 ligose |
| TARDBPTAR DNA binding protein | Dažnai (30–79%) | 1 ligoje |
| TRMT2BtRNA methyltransferase 2B | Dažnai (30–79%) | 1 ligoje |
| UBQLN2ubiquilin 2 | Dažnai (30–79%) | 1 ligoje |
| AASSaminoadipate-semialdehyde synthase | Kartais (5–29%) | 2 ligose |
| CTNNB1catenin beta 1 | Kartais (5–29%) | 1 ligoje |
| FLNAfilamin A | Kartais (5–29%) | 1 ligoje |
| FSD1Lfibronectin type III and SPRY domain containing 1 like | Kartais (5–29%) | 1 ligoje |
| H4C5H4 clustered histone 5 | Kartais (5–29%) | 1 ligoje |
| HSD17B10hydroxysteroid 17-beta dehydrogenase 10 | Kartais (5–29%) | 1 ligoje |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Kartais (5–29%) | 1 ligoje |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Kartais (5–29%) | 1 ligoje |
Rodyti dar 17 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| NTRK2neurotrophic receptor tyrosine kinase 2 | Kartais (5–29%) | 1 ligoje |
| RNU7-1RNA, U7 small nuclear 1 | Kartais (5–29%) | 1 ligoje |
| TANGO2transport and golgi organization 2 homolog | Kartais (5–29%) | 1 ligoje |
| TUBB3tubulin beta 3 class III | Kartais (5–29%) | 1 ligoje |
| PSAPprosaposin | Retai (1–4 %) | 1 ligoje |
| RNU4-2RNA, U4 small nuclear 2 | Retai (1–4 %) | 1 ligoje |
| SPTBN1spectrin beta, non-erythrocytic 1 | Retai (1–4 %) | 1 ligoje |
| ACP5acid phosphatase 5, tartrate resistant | Neužfiksuota | 1 ligoje |
| ADD3adducin 3 | Neužfiksuota | 1 ligoje |
| BCORBCL6 corepressor | Neužfiksuota | 1 ligoje |
| COXFA4cytochrome c oxidase associated subunit FA4 | Neužfiksuota | 1 ligoje |
| GCDHglutaryl-CoA dehydrogenase | Neužfiksuota | 1 ligoje |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Neužfiksuota | 1 ligoje |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Neužfiksuota | 1 ligoje |
| PNPpurine nucleoside phosphorylase | Neužfiksuota | 1 ligoje |
| SIX6SIX homeobox 6 | Neužfiksuota | 1 ligoje |
| SOX2SRY-box transcription factor 2 | 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.
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- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: požymis, jo pavadinimai, apibrėžimas ir su juo susiję genai. Daugiau sužinokite svetainėje hpo.jax.org.
- Duomenų leidimas 2026.10.21-311f020e.
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