Tratto
Noncancerous growth of membranes covering brain
Nome clinico: Meningioma
The presence of a meningioma, i.e., a benign tumor originating from the dura mater or arachnoid mater.
Riepilogo
- Sistema corporeo
- Abnormality of the nervous systemAbnormal tissue mass
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page$trait$nameLeggi i geni collegati a Noncancerous growth of membranes covering brain e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test36 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.
- NeurofibromatosisReads 4 of these genesNF2LZTR1SMARCB1NF1About this report →
- Cerebral Cavernous MalformationReads 3 of these genesCCM2KRIT1PDCD10About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 2 of these genesPTENAKT1About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesSUFUPTCH1About this report →
Show 32 more reports
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 2 of these genesSMARCB1SMARCE1About this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- CEBALID Syndrome (MN1)Reads 1 of these genesMN1About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- NTHL1 Tumour Predisposition SyndromeReads 1 of these genesNTHL1About this report →
- Werner SyndromeReads 1 of these genesWRNAbout this report →
- Malignant Endocrine NeoplasmReads 2 of these genesCDKN1BMEN1About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Coffin-Siris SyndromeReads 2 of these genesSMARCB1SMARCE1About this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesARMC5About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Noonan SyndromeReads 2 of these genesNRASLZTR1About this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFBAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesNTHL1About this report →
- Thyroid CancerReads 2 of these genesMEN1GNASAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 1 of these genesCHEK2About this report →
- Kidney CancerReads 1 of these genesBAP1About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Urinary and Renal System TumourReads 1 of these genesBAP1About this report →
- Intellectual DisabilityReads 4 of these genesCREBBPEIF3FEP300SMARCB1About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesNRASLZTR1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesPTCH1About this report →
- Nephrotic SyndromeReads 1 of these genesCOQ6About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesLMNACOQ6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesCOQ6About this report →
Leggi i geni collegati a Noncancerous growth of membranes covering brain e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test33 geni collegati a Noncancerous growth of membranes covering brain
Alterazioni in questi geni causano malattie rare in cui si osserva Noncancerous growth of membranes covering brain. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| PTENphosphatase and tensin homolog | Sempre | In 5 condizioni |
| WRNWRN RecQ like helicase | Molto spesso (80–99%) | In 2 condizioni |
| LMNAlamin A/C | Spesso (30–79%) | In 1 condizione |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Spesso (30–79%) | In 4 condizioni |
| NTHL1nth like DNA glycosylase 1 | Spesso (30–79%) | In 2 condizioni |
| SUFUSUFU negative regulator of hedgehog signaling | Spesso (30–79%) | In 3 condizioni |
| AKT1AKT serine/threonine kinase 1 | A volte (5–29%) | In 1 condizione |
| BAP1BRCA1 associated deubiquitinase 1 | A volte (5–29%) | In 1 condizione |
| CDKN1Bcyclin dependent kinase inhibitor 1B | A volte (5–29%) | In 1 condizione |
| CDKN2Bcyclin dependent kinase inhibitor 2B | A volte (5–29%) | In 1 condizione |
| CREBBPCREB binding lysine acetyltransferase | A volte (5–29%) | In 2 condizioni |
| EIF3Feukaryotic translation initiation factor 3 subunit F | A volte (5–29%) | In 1 condizione |
| EP300EP300 lysine acetyltransferase | A volte (5–29%) | In 1 condizione |
| MBD4methyl-CpG binding domain 4, DNA glycosylase | A volte (5–29%) | In 1 condizione |
| MEN1menin 1 | A volte (5–29%) | In 1 condizione |
| NRASNRAS proto-oncogene, GTPase | A volte (5–29%) | In 1 condizione |
| PTCH1patched 1 | A volte (5–29%) | In 1 condizione |
| PTCH2patched 2 | A volte (5–29%) | In 1 condizione |
| ARMC5armadillo repeat containing 5 | Raramente (1–4%) | In 1 condizione |
| CCM2CCM2 scaffold protein | Raramente (1–4%) | In 1 condizione |
| COQ6coenzyme Q6, monooxygenase | Raramente (1–4%) | In 1 condizione |
| GNASGNAS complex locus | Raramente (1–4%) | In 1 condizione |
| KDM1Alysine demethylase 1A | Raramente (1–4%) | In 1 condizione |
| KRIT1KRIT1 ankyrin repeat containing | Raramente (1–4%) | In 1 condizione |
| LZTR1leucine zipper like post translational regulator 1 | Raramente (1–4%) | In 1 condizione |
| PDCD10programmed cell death 10 | Raramente (1–4%) | In 1 condizione |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Raramente (1–4%) | In 3 condizioni |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Raramente (1–4%) | In 2 condizioni |
| CHEK2checkpoint kinase 2 | Non registrato | In 1 condizione |
| MN1MN1 proto-oncogene, transcriptional regulator | Non registrato | In 1 condizione |
| NF1neurofibromin 1 | Non registrato | In 1 condizione |
| PDGFBplatelet derived growth factor subunit B | Non registrato | In 1 condizione |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più specifici
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.21-777c9289.
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