Kenmerk
Decreased salivary flow
Klinische naam: Xerostomia
Dryness of the mouth due to salivary gland dysfunction.
Samenvatting
- Ook bekend als
- Dry mouth, Dry mouth syndrome, Reduced salivation
- Lichaamssysteem
- Abnormality of head or neck
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page$trait$nameLees de genen die aan Decreased salivary flow gekoppeld zijn, en de rest van uw genoom, met één test.
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Mijn Genome Test bestellen34 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.
- Amyotrophic Lateral Sclerosis (ALS)Reads 20 of these genesANGANXA11CCNFCHCHD10CHMP2BDCTN1About this report →
- Frontotemporal DementiaReads 7 of these genesCCNFCHCHD10CHMP2BHNRNPA1SQSTM1TBK1About this report →
- Inherited Neurodegenerative DisordersReads 22 of these genesANGANXA11ATXN2CCNFCHCHD10CHMP2BAbout this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
Show 30 more reports
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Distal MyopathiesReads 4 of these genesHNRNPA1LRP12MATR3VCPAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Ectodermal DysplasiasReads 2 of these genesEDARADDTP63About this report →
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesCHCHD10DCTN1FIG4GSNNEFHVCPAbout this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesDCTN1FIG4NEFHVCPAbout this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR2FGFR3About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesCAV1About this report →
- Spinal Muscular AtrophyReads 2 of these genesCHCHD10DCTN1About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesSIM1About this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesMAGEL2About this report →
- Familial HypomagnesemiaReads 1 of these genesCLDN10About this report →
- Hereditary AmyloidosisReads 1 of these genesGSNAbout this report →
- LipodystrophyReads 1 of these genesCAV1About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesGSNAbout this report →
- Autoimmune DiseaseReads 1 of these genesNOD2About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesSCN9AAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesATXN2About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesMAGEL2About this report →
- Female InfertilityReads 1 of these genesTP63About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesTREM2About this report →
- Hearing Loss and DeafnessReads 1 of these genesSLC12A2About this report →
- Epilepsy (Full Panel)Reads 1 of these genesSCN9AAbout this report →
- Intellectual DisabilityReads 1 of these genesERBB4About this report →
Lees de genen die aan Decreased salivary flow gekoppeld zijn, en de rest van uw genoom, met één test.
Vanaf $ 449Gratis verzending · Resultaten binnen 6–8 weken
Mijn Genome Test bestellen53 genen gekoppeld aan Decreased salivary flow
Veranderingen in deze genen veroorzaken zeldzame aandoeningen waarbij Decreased salivary flow voorkomt. De meeste mensen met dit kenmerk hebben geen van die aandoeningen, en een gen op deze lijst zegt niets over het eigen genoom van iemand.
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| CHRM3cholinergic receptor muscarinic 3 | Altijd | In 1 aandoening |
| CLDN10claudin 10 | Altijd | In 1 aandoening |
| EDARADDEDAR associated via death domain | Altijd | In 1 aandoening |
| PLD4phospholipase D family member 4 | Altijd | In 1 aandoening |
| SLC12A2solute carrier family 12 member 2 | Altijd | In 1 aandoening |
| ANGangiogenin | Vaak (30–79%) | In 1 aandoening |
| ANXA11annexin A11 | Vaak (30–79%) | In 1 aandoening |
| ATXN2ataxin 2 | Vaak (30–79%) | In 1 aandoening |
| CAV1caveolin 1 | Vaak (30–79%) | In 1 aandoening |
| CCN2cellular communication network factor 2 | Vaak (30–79%) | In 1 aandoening |
| CCNFcyclin F | Vaak (30–79%) | In 1 aandoening |
| CCR6C-C motif chemokine receptor 6 | Vaak (30–79%) | In 1 aandoening |
| CFAP410cilia and flagella associated protein 410 | Vaak (30–79%) | In 1 aandoening |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Vaak (30–79%) | In 1 aandoening |
| CHMP2Bcharged multivesicular body protein 2B | Vaak (30–79%) | In 1 aandoening |
| DAOD-amino acid oxidase | Vaak (30–79%) | In 1 aandoening |
| DCTN1dynactin subunit 1 | Vaak (30–79%) | In 1 aandoening |
| ELOVL1ELOVL fatty acid elongase 1 | Vaak (30–79%) | In 1 aandoening |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Vaak (30–79%) | In 1 aandoening |
| FGF10fibroblast growth factor 10 | Vaak (30–79%) | In 3 aandoeningen |
| FGFR2fibroblast growth factor receptor 2 | Vaak (30–79%) | In 2 aandoeningen |
| FGFR3fibroblast growth factor receptor 3 | Vaak (30–79%) | In 1 aandoening |
| FIG4FIG4 phosphoinositide 5-phosphatase | Vaak (30–79%) | In 1 aandoening |
| FUSFUS RNA binding protein | Vaak (30–79%) | In 1 aandoening |
| GLE1GLE1 RNA export mediator | Vaak (30–79%) | In 1 aandoening |
| GLT8D1glycosyltransferase 8 domain containing 1 | Vaak (30–79%) | In 1 aandoening |
| GSNgelsolin | Vaak (30–79%) | In 1 aandoening |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Vaak (30–79%) | In 1 aandoening |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Vaak (30–79%) | In 1 aandoening |
| IRF5interferon regulatory factor 5 | Vaak (30–79%) | In 1 aandoening |
| LBRlamin B receptor | Vaak (30–79%) | In 1 aandoening |
| LRP12LDL receptor related protein 12 | Vaak (30–79%) | In 1 aandoening |
| MATR3matrin 3 | Vaak (30–79%) | In 1 aandoening |
| NEFHneurofilament heavy chain | Vaak (30–79%) | In 1 aandoening |
| NEK1NIMA related kinase 1 | Vaak (30–79%) | In 1 aandoening |
| OPTNoptineurin | Vaak (30–79%) | In 1 aandoening |
| PFN1profilin 1 | Vaak (30–79%) | In 1 aandoening |
| PRPHperipherin | Vaak (30–79%) | In 1 aandoening |
| SOD1superoxide dismutase 1 | Vaak (30–79%) | In 1 aandoening |
| SQSTM1sequestosome 1 | Vaak (30–79%) | In 1 aandoening |
Toon nog 13 genen
| Gen | Hoe vaak het voorkomt | Aandoeningen |
|---|---|---|
| TAF15TATA-box binding protein associated factor 15 | Vaak (30–79%) | In 1 aandoening |
| TARDBPTAR DNA binding protein | Vaak (30–79%) | In 1 aandoening |
| TBK1TANK binding kinase 1 | Vaak (30–79%) | In 1 aandoening |
| TREM2triggering receptor expressed on myeloid cells 2 | Vaak (30–79%) | In 1 aandoening |
| UBQLN2ubiquilin 2 | Vaak (30–79%) | In 1 aandoening |
| UNC13Aunc-13 homolog A | Vaak (30–79%) | In 1 aandoening |
| VAPBVAMP associated protein B and C | Vaak (30–79%) | In 1 aandoening |
| VCPvalosin containing protein | Vaak (30–79%) | In 1 aandoening |
| MAGEL2MAGE family member L2 | Soms (5–29%) | In 1 aandoening |
| NOD2nucleotide binding oligomerization domain containing 2 | Soms (5–29%) | In 2 aandoeningen |
| SIM1SIM bHLH transcription factor 1 | Soms (5–29%) | In 1 aandoening |
| TP63tumor protein p63 | Soms (5–29%) | In 2 aandoeningen |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Niet vastgelegd | In 1 aandoening |
Hoe vaak dit voorkomt bij mensen met een van de aandoeningen van het gen, de hoogste frequentie binnen die aandoeningen, zoals de Human Phenotype Ontology dit vastlegt. Deze pagina's beschrijven kenmerken en het onderzoek erachter; het zijn geen diagnose, en over symptomen kunt u het best een arts of genetisch adviseur raadplegen.
Bredere kenmerken
Waar dit vandaan komt
- De Human Phenotype Ontology, release 2026-09-01: het kenmerk, de namen, de definitie en de genen die ermee verbonden zijn. Meer informatie vindt u op hpo.jax.org.
- Gegevensrelease 2026.10.19-9814e911.
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