Požymis
Small hippocampus
Klinikinis pavadinimas: Hypoplastic hippocampus
Underdevelopment of the hippocampus.
Santrauka
- Taip pat vadinama
- Underdeveloped hippocampus
- Kūno sistema
- Abnormality of the nervous 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/hypoplastic-hippocampus.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Small hippocampus, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test20 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.
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- EML1-Related Band HeterotopiaReads 1 of these genesEML1About this report →
- MTHFD1 DeficiencyReads 1 of these genesMTHFD1About this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
Show 16 more reports
- Familial Hemiplegic MigraineReads 1 of these genesSCN1AAbout this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- TubulinopathiesReads 1 of these genesTUBA1AAbout this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesNDE1TUBA1AAbout this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesTUBA1AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATP1A3CAMTA1About this report →
- Epilepsy (Full Panel)Reads 4 of these genesSCN1AATP1A3GRIN1SLC35A2About this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBA1AAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesATP1A3About this report →
- Inherited Neurodegenerative DisordersReads 3 of these genesATP1A3VPS13ACAMTA1About this report →
- Intellectual DisabilityReads 2 of these genesTCF4GRIN1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesSLC35A2About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesCARS2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesVPS13AAbout this report →
Vienu tyrimu sužinokite genus, susijusius su Small hippocampus, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test19 genų susiję su Small hippocampus
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Small hippocampus. 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 |
|---|---|---|
| CLCN3Cl-/H+ antiporter 3 | Visada | 1 ligoje |
| MTHFD1methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 | Visada | 1 ligoje |
| VPS51VPS51 subunit of GARP complex | Visada | 1 ligoje |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Labai dažnai (80–99%) | 1 ligoje |
| STAMBPSTAM binding protein | Labai dažnai (80–99%) | 1 ligoje |
| BORCS5BLOC-1 related complex subunit 5 | Dažnai (30–79%) | 1 ligoje |
| EML1EMAP like 1 | Dažnai (30–79%) | 1 ligoje |
| NDE1nudE neurodevelopment protein 1 | Dažnai (30–79%) | 1 ligoje |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Dažnai (30–79%) | 1 ligoje |
| TCF4transcription factor 4 | Dažnai (30–79%) | 1 ligoje |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Kartais (5–29%) | 1 ligoje |
| CARS2cysteinyl-tRNA synthetase 2, mitochondrial | Kartais (5–29%) | 1 ligoje |
| GRIN1glutamate ionotropic receptor NMDA type subunit 1 | Kartais (5–29%) | 1 ligoje |
| TUBA1Atubulin alpha 1a | Kartais (5–29%) | 1 ligoje |
| VPS13Avacuolar protein sorting 13 homolog A | Kartais (5–29%) | 1 ligoje |
| WSB2WD repeat and SOCS box containing 2 | Kartais (5–29%) | 1 ligoje |
| CAMTA1calmodulin binding transcription activator 1 | Retai (1–4 %) | 1 ligoje |
| POU4F1POU class 4 homeobox 1 | Retai (1–4 %) | 1 ligoje |
| SLC35A2solute carrier family 35 member A2 | Retai (1–4 %) | 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.
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 2026.10.19-9814e911.
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