Požymis
Communicating hydrocephalus
A form of hydrocephalus in which there is no visible obstruction to the flow of the cerebrospinal fluid between the ventricles and subarachnoid space.
Santrauka
- 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/communicating-hydrocephalus.json"
page <- fromJSON(url)
page$trait$nameVienu tyrimu sužinokite genus, susijusius su Communicating hydrocephalus, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test18 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.
- Dyskeratosis CongenitaReads 4 of these genesCDCA7DNMT3BHELLSZBTB24About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Marfan Like SyndromesReads 2 of these genesFBN1SKIAbout this report →
- Osteogenesis ImperfectaReads 3 of these genesP4HBCRTAPSEC24DAbout this report →
Show 14 more reports
- PancreatitisReads 1 of these genesTRPV6About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesMAN2B1About this report →
- Classic Organic AciduriasReads 1 of these genesGCDHAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesTRNT1About this report →
- Familial HypomagnesemiaReads 1 of these genesTRPV6About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesRNU4-2About this report →
- Syndromic CraniosynostosisReads 1 of these genesSKIAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesB4GAT1About this report →
- Thyroid CancerReads 1 of these genesTRPV6About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesSLC2A1About this report →
- Primary Ciliary DyskinesiaReads 1 of these genesDNAI1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesMAN2B1About this report →
- Epilepsy (Full Panel)Reads 1 of these genesSLC2A1About this report →
Vienu tyrimu sužinokite genus, susijusius su Communicating hydrocephalus, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test24 genų susiję su Communicating hydrocephalus
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Communicating hydrocephalus. 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 |
|---|---|---|
| P4HBprolyl 4-hydroxylase subunit beta | Visada | 2 ligose |
| TRIM71tripartite motif containing 71 | Visada | 1 ligoje |
| B4GAT1beta-1,4-glucuronyltransferase 1 | Dažnai (30–79%) | 1 ligoje |
| CDCA7cell division cycle associated 7 | Dažnai (30–79%) | 1 ligoje |
| CRTAPcartilage associated protein | Dažnai (30–79%) | 1 ligoje |
| DLG5discs large MAGUK scaffold protein 5 | Dažnai (30–79%) | 1 ligoje |
| DNMT3BDNA methyltransferase 3 beta | Dažnai (30–79%) | 1 ligoje |
| FBN1fibrillin 1 | Dažnai (30–79%) | 1 ligoje |
| GCDHglutaryl-CoA dehydrogenase | Dažnai (30–79%) | 1 ligoje |
| HELLShelicase, lymphoid specific | Dažnai (30–79%) | 1 ligoje |
| HERC1HECT and RLD domain containing E3 ubiquitin protein ligase family member 1 | Dažnai (30–79%) | 2 ligose |
| PTENphosphatase and tensin homolog | Dažnai (30–79%) | 1 ligoje |
| SEC24DSEC24 homolog D, COPII component | Dažnai (30–79%) | 1 ligoje |
| SKISKI proto-oncogene | Dažnai (30–79%) | 1 ligoje |
| UHRF1ubiquitin like with PHD and ring finger domains 1 | Dažnai (30–79%) | 1 ligoje |
| ZBTB24zinc finger and BTB domain containing 24 | Dažnai (30–79%) | 1 ligoje |
| CDC42BPBCDC42 binding protein kinase beta | Kartais (5–29%) | 1 ligoje |
| SLC2A1solute carrier family 2 member 1 | Kartais (5–29%) | 1 ligoje |
| TRNT1tRNA nucleotidyl transferase 1 | Kartais (5–29%) | 1 ligoje |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Kartais (5–29%) | 1 ligoje |
| MAN2B1mannosidase alpha class 2B member 1 | Retai (1–4 %) | 1 ligoje |
| RNU4-2RNA, U4 small nuclear 2 | Retai (1–4 %) | 1 ligoje |
| DNAI1dynein axonemal intermediate chain 1 | Neužfiksuota | 1 ligoje |
| MPDZmultiple PDZ domain crumbs cell polarity complex component | 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.
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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