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Merkmal
Dizziness
Klinische Bezeichnung: Vertigo
An abnormal sensation of spinning while the body is actually stationary.
Zusammenfassung
- Auch genannt
- Dizzy spell
- Körpersystem
- Abnormality of the ear
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Diese Seite als Daten
Hängen Sie .json an die Adresse der Seite an oder fordern Sie application/json an, um sie als JSON zu lesen.
library(jsonlite)
url <- "https://dantelabs.com/traits/vertigo.json"
page <- fromJSON(url)
page$trait$nameDizzinessHP:0002321
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Lesen Sie die Gene aus, die mit Dizziness zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen89 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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- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 3 of these genesIFNGR1IL12BIL23RAbout this report →
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- Urinary and Renal System TumourReads 3 of these genesSDHATP53VHLAbout this report →
- Inherited Congenital Heart DefectsReads 3 of these genesGATA4GATA6NKX2-5About this report →
- Hereditary Periodic Fever SyndromesReads 2 of these genesTNFRSF1AMVKAbout this report →
- Renal Tubular AcidosisReads 2 of these genesATP6V1B1FOXI1About this report →
- PolycythemiaReads 2 of these genesEPORVHLAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesSCN5ATRPM4About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesSUFUAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 4 of these genesCACNA1ACACNA1GFGF14NOP56About this report →
- Kidney CancerReads 2 of these genesTP53VHLAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 2 of these genesSDHAVHLAbout this report →
- Other Inborn Errors of ImmunityReads 9 of these genesGATA2IRF2BP2MYD88STAT3TET2C4AAbout this report →
- Familial HypomagnesemiaReads 2 of these genesCNNM2KCNJ10About this report →
- Usher SyndromeReads 2 of these genesCDH23MYO7AAbout this report →
- Familial Periodic ParalysisReads 1 of these genesKCNJ2About this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Dilated CardiomyopathyReads 4 of these genesEMDABCC9SCN5ATTNAbout this report →
- Myofibrillar MyopathiesReads 2 of these genesRYR1TTNAbout this report →
- Thyroid CancerReads 3 of these genesNKX2-5MEN1SLC26A4About this report →
- Inherited ThrombocytopeniasReads 3 of these genesMPLFLI1THPOAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesGATA2About this report →
- NeurofibromatosisReads 1 of these genesNF2About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesTPK1About this report →
- Congenital HypothyroidismReads 2 of these genesNKX2-5SLC26A4About this report →
- Congenital MyopathiesReads 2 of these genesRYR1TTNAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Bartter DiseaseReads 1 of these genesCLCNKBAbout this report →
- Autoimmune DiseaseReads 2 of these genesSTAT3FASAbout this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesSTAT5BAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Hearing Loss and DeafnessReads 4 of these genesCDH23SLC26A4COCHMYO7AAbout this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesNAGAAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesFASAbout this report →
- Catecholaminergic Polymorphic Ventricular TachycardiaReads 1 of these genesCALM1About this report →
- Classic Organic AciduriasReads 1 of these genesGCDHAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Diabetes MellitusReads 2 of these genesGATA4GATA6About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesPRRT2KCNJ10About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesPITX2About this report →
- Intellectual DisabilityReads 5 of these genesSCN2ASRPK3TBL1XR1MED12CTNNB1About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesIRF2BP2About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesJUPAbout this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesDBHAbout this report →
- Lysosomal Storage DiseaseReads 2 of these genesNAGAGLAAbout this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesBRAFMYL2About this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC4AAbout this report →
- Leigh SyndromeReads 2 of these genesSDHATPK1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesGATA4About this report →
- Distal MyopathiesReads 1 of these genesTTNAbout this report →
- Epidermolysis BullosaReads 1 of these genesJUPAbout this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesNPM1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTTNAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesADA2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesTRPM4About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesSUFUAbout this report →
- Hypogonadotropic HypogonadismReads 1 of these genesNR0B1About this report →
Lesen Sie die Gene aus, die mit Dizziness zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen140 Gene mit Dizziness verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Dizziness auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Immer | In 1 Erkrankung |
| EMDemerin | Immer | In 1 Erkrankung |
| FDXRferredoxin reductase | Immer | In 1 Erkrankung |
| GCGRglucagon receptor | Immer | In 1 Erkrankung |
| LAMB1laminin subunit beta 1 | Immer | In 1 Erkrankung |
| MAU2MAU2 sister chromatid cohesion factor | Immer | In 1 Erkrankung |
| NOTCH3notch receptor 3 | Immer | In 1 Erkrankung |
| RFC4replication factor C subunit 4 | Immer | In 1 Erkrankung |
| RRP12ribosomal RNA processing 12 homolog | Immer | In 2 Erkrankungen |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Immer | In 2 Erkrankungen |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Immer | In 1 Erkrankung |
| ADA2adenosine deaminase 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Sehr häufig (80–99 %) | In 6 Erkrankungen |
| EPORerythropoietin receptor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| JAK2Janus kinase 2 | Sehr häufig (80–99 %) | In 4 Erkrankungen |
| JUPjunction plakoglobin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NAGAalpha-N-acetylgalactosaminidase | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| SLC1A3solute carrier family 1 member 3 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| ABCC9ATP binding cassette subfamily C member 9 | Häufig (30–79 %) | In 1 Erkrankung |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| BCORBCL6 corepressor | Häufig (30–79 %) | In 1 Erkrankung |
| CACNB4calcium voltage-gated channel auxiliary subunit beta 4 | Häufig (30–79 %) | In 2 Erkrankungen |
| CALRcalreticulin | Häufig (30–79 %) | In 1 Erkrankung |
| CCND1cyclin D1 | Häufig (30–79 %) | In 2 Erkrankungen |
| CMPK2cytidine/uridine monophosphate kinase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| DKK1dickkopf Wnt signaling pathway inhibitor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Häufig (30–79 %) | In 1 Erkrankung |
| GATA2GATA binding protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| GATA4GATA binding protein 4 | Häufig (30–79 %) | In 1 Erkrankung |
| GATA5GATA binding protein 5 | Häufig (30–79 %) | In 1 Erkrankung |
| GATA6GATA binding protein 6 | Häufig (30–79 %) | In 1 Erkrankung |
| GJA5gap junction protein alpha 5 | Häufig (30–79 %) | In 1 Erkrankung |
| GYG1glycogenin 1 | Häufig (30–79 %) | In 1 Erkrankung |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| JAM2junctional adhesion molecule 2 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| KCNA5potassium voltage-gated channel subfamily A member 5 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNE1potassium voltage-gated channel subfamily E regulatory subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNE2potassium voltage-gated channel subfamily E regulatory subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Häufig (30–79 %) | In 1 Erkrankung |
100 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| KCNJ3potassium inwardly rectifying channel subfamily J member 3 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Häufig (30–79 %) | In 1 Erkrankung |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| LRP4LDL receptor related protein 4 | Häufig (30–79 %) | In 1 Erkrankung |
| MPLMPL proto-oncogene, thrombopoietin receptor | Häufig (30–79 %) | In 2 Erkrankungen |
| MYD88MYD88 innate immune signal transduction adaptor | Häufig (30–79 %) | In 1 Erkrankung |
| MYL4myosin light chain 4 | Häufig (30–79 %) | In 1 Erkrankung |
| MYORGmyogenesis regulating glycosidase | Häufig (30–79 %) | In 1 Erkrankung |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Häufig (30–79 %) | In 1 Erkrankung |
| NABP1nucleic acid binding protein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| NKX2-5NK2 homeobox 5 | Häufig (30–79 %) | In 2 Erkrankungen |
| NKX2-6NK2 homeobox 6 | Häufig (30–79 %) | In 1 Erkrankung |
| NPM1nucleophosmin 1 | Häufig (30–79 %) | In 1 Erkrankung |
| NPPAnatriuretic peptide A | Häufig (30–79 %) | In 2 Erkrankungen |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| NUMA1nuclear mitotic apparatus protein 1 | Häufig (30–79 %) | In 1 Erkrankung |
| NUP155nucleoporin 155 | Häufig (30–79 %) | In 1 Erkrankung |
| PDGFBplatelet derived growth factor subunit B | Häufig (30–79 %) | In 2 Erkrankungen |
| PDGFRBplatelet derived growth factor receptor beta | Häufig (30–79 %) | In 1 Erkrankung |
| PITX2paired like homeodomain 2 | Häufig (30–79 %) | In 1 Erkrankung |
| PMLPML nuclear body scaffold | Häufig (30–79 %) | In 1 Erkrankung |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Häufig (30–79 %) | In 1 Erkrankung |
| PRRT2proline rich transmembrane protein 2 | Häufig (30–79 %) | In 1 Erkrankung |
| RARAretinoic acid receptor alpha | Häufig (30–79 %) | In 1 Erkrankung |
| RYR1ryanodine receptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN3Bsodium voltage-gated channel beta subunit 3 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN4Bsodium voltage-gated channel beta subunit 4 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Häufig (30–79 %) | In 3 Erkrankungen |
| SH2B3SH2B adaptor protein 3 | Häufig (30–79 %) | In 2 Erkrankungen |
| SLC20A2solute carrier family 20 member 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SRPK3SRSF protein kinase 3 | Häufig (30–79 %) | In 1 Erkrankung |
| STAT3signal transducer and activator of transcription 3 | Häufig (30–79 %) | In 1 Erkrankung |
| STAT5Bsignal transducer and activator of transcription 5B | Häufig (30–79 %) | In 1 Erkrankung |
| SUFUSUFU negative regulator of hedgehog signaling | Häufig (30–79 %) | In 1 Erkrankung |
| TBL1XR1TBL1X/Y related 1 | Häufig (30–79 %) | In 1 Erkrankung |
| TET2tet methylcytosine dioxygenase 2 | Häufig (30–79 %) | In 1 Erkrankung |
| TP53tumor protein p53 | Häufig (30–79 %) | In 1 Erkrankung |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Häufig (30–79 %) | In 1 Erkrankung |
| TTNtitin | Häufig (30–79 %) | In 1 Erkrankung |
| VHLvon Hippel-Lindau tumor suppressor | Häufig (30–79 %) | In 2 Erkrankungen |
| VSX1visual system homeobox 1 | Häufig (30–79 %) | In 1 Erkrankung |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ZBTB16zinc finger and BTB domain containing 16 | Häufig (30–79 %) | In 1 Erkrankung |
| AIPAHR interacting HSP90 co-chaperone | Manchmal (5–29 %) | In 1 Erkrankung |
| C4Acomplement C4A (Chido/Rodgers blood group) | Manchmal (5–29 %) | In 1 Erkrankung |
| CACNA1Gcalcium voltage-gated channel subunit alpha1 G | Manchmal (5–29 %) | In 1 Erkrankung |
| CCR1C-C motif chemokine receptor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| CDH23cadherin related 23 | Manchmal (5–29 %) | In 2 Erkrankungen |
| CHD2chromodomain helicase DNA binding protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CNNM2cyclin and CBS domain divalent metal cation transport mediator 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CUX2cut like homeobox 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| DBHdopamine beta-hydroxylase | Manchmal (5–29 %) | In 1 Erkrankung |
| DNM1dynamin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| FASFas cell surface death receptor | Manchmal (5–29 %) | In 2 Erkrankungen |
| FGF14fibroblast growth factor 14 | Manchmal (5–29 %) | In 1 Erkrankung |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Manchmal (5–29 %) | In 1 Erkrankung |
| FOXI1forkhead box I1 | Manchmal (5–29 %) | In 1 Erkrankung |
| GABRB3gamma-aminobutyric acid type A receptor subunit beta3 | Manchmal (5–29 %) | In 1 Erkrankung |
| GCDHglutaryl-CoA dehydrogenase | Manchmal (5–29 %) | In 1 Erkrankung |
| GLAgalactosidase alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| HLA-Bmajor histocompatibility complex, class I, B | Manchmal (5–29 %) | In 3 Erkrankungen |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| IFNGR1interferon gamma receptor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| IL10interleukin 10 | Manchmal (5–29 %) | In 1 Erkrankung |
| IL12Ainterleukin 12A | Manchmal (5–29 %) | In 1 Erkrankung |
| IL12A-AS1IL12A antisense RNA 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| IL12Binterleukin 12B | Manchmal (5–29 %) | In 1 Erkrankung |
| IL23Rinterleukin 23 receptor | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNQ2potassium voltage-gated channel subfamily Q member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| KLRC4killer cell lectin like receptor C4 | Manchmal (5–29 %) | In 1 Erkrankung |
| MAPK10mitogen-activated protein kinase 10 | Manchmal (5–29 %) | In 1 Erkrankung |
| MED12mediator complex subunit 12 | Manchmal (5–29 %) | In 1 Erkrankung |
| MEFVMEFV innate immunity regulator, pyrin | Manchmal (5–29 %) | In 1 Erkrankung |
| MEN1menin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| MLXMAX dimerization protein MLX | Manchmal (5–29 %) | In 1 Erkrankung |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Manchmal (5–29 %) | In 1 Erkrankung |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Manchmal (5–29 %) | In 2 Erkrankungen |
| SLC26A4solute carrier family 26 member 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| STAT4signal transducer and activator of transcription 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| THPOthrombopoietin | Manchmal (5–29 %) | In 1 Erkrankung |
| TLR4toll like receptor 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| TNFRSF1ATNF receptor superfamily member 1A | Manchmal (5–29 %) | In 1 Erkrankung |
| UBAC2UBA domain containing 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Selten (1–4 %) | In 1 Erkrankung |
| CLCNKBchloride voltage-gated channel Kb | Selten (1–4 %) | In 1 Erkrankung |
| CTNNB1catenin beta 1 | Selten (1–4 %) | In 1 Erkrankung |
| NOP56NOP56 ribonucleoprotein | Selten (1–4 %) | In 1 Erkrankung |
| SLC12A3solute carrier family 12 member 3 | Selten (1–4 %) | In 2 Erkrankungen |
| CALM1calmodulin 1 | Nicht erfasst | In 1 Erkrankung |
| COCHcochlin | Nicht erfasst | In 1 Erkrankung |
| MVKmevalonate kinase | Nicht erfasst | In 1 Erkrankung |
| MYL2myosin light chain 2 | Nicht erfasst | In 1 Erkrankung |
| MYO7Amyosin VIIA | Nicht erfasst | In 2 Erkrankungen |
| TPK1thiamin pyrophosphokinase 1 | Nicht erfasst | In 1 Erkrankung |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Untergeordnete Merkmale
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.17-8666dff2.
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