AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Abdominal bloating
Klinikinis pavadinimas: Abdominal distention
Distention of the abdomen.
Santrauka
- Taip pat vadinama
- Abdominal swelling, Belly bloating, Bloating, Abdominal distension, Distended abdomen
- Kūno sistema
- Abnormality of the digestive system
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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/abdominal-distention.json"
page <- fromJSON(url)
page$trait$nameAbdominal bloatingHP:0003270
AtlasKam padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Abdominal bloating, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test109 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.
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 6 of these genesMYH11MYL9ACTG2MYLKERBB3FLNAAbout this report →
- Hereditary SpherocytosisReads 5 of these genesANK1EPB42SLC4A1SPTA1SPTBAbout this report →
- Polycystic Liver Disease (1 and 2)Reads 4 of these genesALG8LRP5PRKCSHSEC63About this report →
- Congenital Diarrhoeas & EnteropathiesReads 7 of these genesSLC9A3STX3EPCAMMYO5BSLC5A1SLC26A3About this report →
Show 105 more reports
- Achondrogenesis panelReads 3 of these genesCOL2A1TRIP11SLC26A2About this report →
- Hereditary Episodic AtaxiasReads 3 of these genesCACNA1ASCN2ASLC1A3About this report →
- Congenital Intestinal Atresia & Short BowelReads 2 of these genesCLMPTTC7AAbout this report →
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- Congenital HypothyroidismReads 6 of these genesFOXE1NKX2-1NKX2-5PAX8SLC26A4TSHRAbout this report →
- Disorder of Copper MetabolismReads 2 of these genesATP7BATP7AAbout this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesPHOX2BRETAbout this report →
- Red Blood Cell Membrane DisordersReads 3 of these genesSLC4A1SPTA1SPTBAbout this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Asphyxiating Thoracic Dystrophy 2 (IFT80)Reads 1 of these genesIFT80About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Glucose-Galactose MalabsorptionReads 1 of these genesSLC5A1About this report →
- Jeune Asphyxiating Thoracic Dystrophy (DYNC2H1)Reads 1 of these genesDYNC2H1About this report →
- Lysosomal Acid Lipase Deficiency (Wolman Disease and CESD)Reads 1 of these genesLIPAAbout this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Pendred SyndromeReads 1 of these genesSLC26A4About this report →
- PLEC-Related Epidermolysis Bullosa and Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Polycystic Ovary SyndromeReads 1 of these genesFSHRAbout this report →
- Short-Rib Thoracic Dysplasia 11 (DYNC2I2)Reads 1 of these genesDYNC2I2About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Short-Rib Thoracic Dysplasia 8 (DYNC2I1)Reads 1 of these genesDYNC2I1About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Thyroid CancerReads 5 of these genesNKX2-5PAX8SLC26A4TSHRRETAbout this report →
- Waardenburg SyndromeReads 2 of these genesEDN3EDNRBAbout this report →
- Epilepsy (Full Panel)Reads 10 of these genesPIGAATP1A2ATP1A3CACNA1AHACE1RHOBTB2About this report →
- Hepatic Porphyria DisordersReads 2 of these genesALADHMBSAbout this report →
- Congenital Disaccharidase DeficienciesReads 1 of these genesSIAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA1About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- TRIP11-Related Skeletal DysplasiaReads 1 of these genesTRIP11About this report →
- Epidermolysis BullosaReads 3 of these genesITGA6ITGB4PLECAbout this report →
- Primary Mitochondrial DiseaseReads 8 of these genesPOLG2LIG3POLGRRM2BTYMPC2orf69About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1SLC26A2About this report →
- PorphyriaReads 2 of these genesALADHMBSAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 10 of these genesTRMULIG3POLGRRM2BTYMPATP7AAbout this report →
- Meckel SyndromeReads 2 of these genesTXNDC15TCTN2About this report →
- Fraser SyndromeReads 1 of these genesFREM2About this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesALDOBAbout this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesSMARCAL1About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Aortic AneurysmReads 2 of these genesMYH11MYLKAbout this report →
- Inherited Congenital Heart DefectsReads 2 of these genesNKX2-5FLNAAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesLIPASMPD1ARSAPSAPAbout this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC2A2PYGLAbout this report →
- Hereditary Vascular MalformationsReads 1 of these genesEPHB4About this report →
- Neonatal Diabetes MellitusReads 2 of these genesMNX1SLC2A2About this report →
- Lynch SyndromeReads 1 of these genesEPCAMAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Syndromic CraniosynostosisReads 2 of these genesWDR35SMOAbout this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesPOLGABCD1ATP1A3ATP7ACACNA1AHACE1About this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Systemic Lupus ErythematosusReads 1 of these genesSAT1About this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGAALG8DLL3MESP2About this report →
- VitreoretinopathyReads 2 of these genesCOL2A1LRP5About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR35About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesSAR1BAbout this report →
- Diabetes MellitusReads 2 of these genesMNX1SLC2A2About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesPLECTNPO3About this report →
- Other Inherited LeukodystrophiesReads 3 of these genesABCD1ARSAPSAPAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesATP1A3CACNA1AAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesATP1A3SLC2A1About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Familial Intrahepatic CholestasisReads 1 of these genesMYO5BAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG8About this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- OsteopetrosisReads 1 of these genesLRP5About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesEPHB4About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesABCD1HACE1About this report →
- Fanconi AnemiaReads 1 of these genesBRCA1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP7AMPV17About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Autoimmune DiseaseReads 1 of these genesSAT1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Intellectual DisabilityReads 3 of these genesSCN2ACHD8ZEB2About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPLECAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Nephrotic SyndromeReads 1 of these genesNPHS1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesTCTN2About this report →
- DNA Repair DiseaseReads 1 of these genesBRCA1About this report →
- Female InfertilityReads 1 of these genesFSHRAbout this report →
- Leigh SyndromeReads 1 of these genesTRMUAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesSLC26A4About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesSMARCAL1About this report →
Vienu tyrimu sužinokite genus, susijusius su Abdominal bloating, ir kitą jūsų genomo dalį.
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Įsigyti savo Genome Test135 genų susiję su Abdominal bloating
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Abdominal bloating. 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 |
|---|---|---|
| ATP7BATPase copper transporting beta | Visada | 1 ligoje |
| CLMPCXADR like cell adhesion molecule | Visada | 1 ligoje |
| DHCR77-dehydrocholesterol reductase | Visada | 1 ligoje |
| LIPAlipase A, lysosomal acid type | Visada | 2 ligose |
| LMOD1leiomodin 1 | Visada | 2 ligose |
| MYH11myosin heavy chain 11 | Visada | 2 ligose |
| MYL9myosin light chain 9 | Visada | 1 ligoje |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Visada | 1 ligoje |
| PLD4phospholipase D family member 4 | Visada | 1 ligoje |
| POLG2DNA polymerase gamma 2, accessory subunit | Visada | 1 ligoje |
| SLC9A3solute carrier family 9 member A3 | Visada | 1 ligoje |
| STX3syntaxin 3 | Visada | 2 ligose |
| TRMUtRNA mitochondrial 2-thiouridylase | Visada | 1 ligoje |
| TXNDC15thioredoxin domain containing 15 | Visada | 1 ligoje |
| ACTG2actin gamma 2, smooth muscle | Labai dažnai (80–99%) | 3 ligose |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Labai dažnai (80–99%) | 2 ligose |
| BRCA1BRCA1 DNA repair associated | Labai dažnai (80–99%) | 1 ligoje |
| COL2A1collagen type II alpha 1 chain | Labai dažnai (80–99%) | 1 ligoje |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Labai dažnai (80–99%) | 1 ligoje |
| DYNC2I1dynein 2 intermediate chain 1 | Labai dažnai (80–99%) | 1 ligoje |
| DYNC2I2dynein 2 intermediate chain 2 | Labai dažnai (80–99%) | 1 ligoje |
| EWSR1EWS RNA binding protein 1 | Labai dažnai (80–99%) | 1 ligoje |
| FOXE1forkhead box E1 | Labai dažnai (80–99%) | 1 ligoje |
| FSHRfollicle stimulating hormone receptor | Labai dažnai (80–99%) | 1 ligoje |
| IFT80intraflagellar transport 80 | Labai dažnai (80–99%) | 1 ligoje |
| ITGA6integrin subunit alpha 6 | Labai dažnai (80–99%) | 1 ligoje |
| ITGB4integrin subunit beta 4 | Labai dažnai (80–99%) | 2 ligose |
| LIG3DNA ligase 3 | Labai dažnai (80–99%) | 1 ligoje |
| LRP5LDL receptor related protein 5 | Labai dažnai (80–99%) | 1 ligoje |
| MYLKmyosin light chain kinase | Labai dažnai (80–99%) | 1 ligoje |
| NKX2-1NK2 homeobox 1 | Labai dažnai (80–99%) | 1 ligoje |
| NKX2-5NK2 homeobox 5 | Labai dažnai (80–99%) | 2 ligose |
| PAX8paired box 8 | Labai dažnai (80–99%) | 4 ligose |
| POLGDNA polymerase gamma, catalytic subunit | Labai dažnai (80–99%) | 2 ligose |
| PRKCSHPRKCSH beta subunit of glucosidase II | Labai dažnai (80–99%) | 2 ligose |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Labai dažnai (80–99%) | 1 ligoje |
| SEC63SEC63 protein translocation regulator | Labai dažnai (80–99%) | 1 ligoje |
| SLC26A4solute carrier family 26 member 4 | Labai dažnai (80–99%) | 2 ligose |
| TRIP11thyroid hormone receptor interactor 11 | Labai dažnai (80–99%) | 1 ligoje |
| TSHRthyroid stimulating hormone receptor | Labai dažnai (80–99%) | 2 ligose |
Rodyti dar 95 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| TYMPthymidine phosphorylase | Labai dažnai (80–99%) | 1 ligoje |
| WDR35WD repeat domain 35 | Labai dažnai (80–99%) | 1 ligoje |
| WT1WT1 transcription factor | Labai dažnai (80–99%) | 1 ligoje |
| ABCD1ATP binding cassette subfamily D member 1 | Dažnai (30–79%) | 1 ligoje |
| ALKALK receptor tyrosine kinase | Dažnai (30–79%) | 1 ligoje |
| ANO1anoctamin 1 | Dažnai (30–79%) | 1 ligoje |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Dažnai (30–79%) | 1 ligoje |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Dažnai (30–79%) | 1 ligoje |
| ATP7AATPase copper transporting alpha | Dažnai (30–79%) | 1 ligoje |
| C2orf69chromosome 2 open reading frame 69 | Dažnai (30–79%) | 1 ligoje |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Dažnai (30–79%) | 1 ligoje |
| COX11cytochrome c oxidase copper chaperone COX11 | Dažnai (30–79%) | 1 ligoje |
| DYMdymeclin | Dažnai (30–79%) | 1 ligoje |
| ECE1endothelin converting enzyme 1 | Dažnai (30–79%) | 1 ligoje |
| EDN3endothelin 3 | Dažnai (30–79%) | 1 ligoje |
| EDNRBendothelin receptor type B | Dažnai (30–79%) | 1 ligoje |
| EPCAMepithelial cell adhesion molecule | Dažnai (30–79%) | 1 ligoje |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Dažnai (30–79%) | 1 ligoje |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Dažnai (30–79%) | 1 ligoje |
| FOCADfocadhesin | Dažnai (30–79%) | 1 ligoje |
| GDNFglial cell derived neurotrophic factor | Dažnai (30–79%) | 1 ligoje |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Dažnai (30–79%) | 1 ligoje |
| INSRinsulin receptor | Dažnai (30–79%) | 2 ligose |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Dažnai (30–79%) | 1 ligoje |
| LMO1LIM domain only 1 | Dažnai (30–79%) | 1 ligoje |
| MNX1motor neuron and pancreas homeobox 1 | Dažnai (30–79%) | 2 ligose |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Dažnai (30–79%) | 1 ligoje |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Dažnai (30–79%) | 1 ligoje |
| MYO5Bmyosin VB | Dažnai (30–79%) | 1 ligoje |
| NRTNneurturin | Dažnai (30–79%) | 1 ligoje |
| PHOX2Bpaired like homeobox 2B | Dažnai (30–79%) | 1 ligoje |
| PI4KAphosphatidylinositol 4-kinase alpha | Dažnai (30–79%) | 1 ligoje |
| PLECplectin | Dažnai (30–79%) | 1 ligoje |
| RETret proto-oncogene | Dažnai (30–79%) | 2 ligose |
| RHOBTB2Rho related BTB domain containing 2 | Dažnai (30–79%) | 1 ligoje |
| SAR1Bsecretion associated Ras related GTPase 1B | Dažnai (30–79%) | 1 ligoje |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Dažnai (30–79%) | 1 ligoje |
| SEMA3Csemaphorin 3C | Dažnai (30–79%) | 1 ligoje |
| SEMA3Dsemaphorin 3D | Dažnai (30–79%) | 1 ligoje |
| SLC1A3solute carrier family 1 member 3 | Dažnai (30–79%) | 1 ligoje |
| SLC2A1solute carrier family 2 member 1 | Dažnai (30–79%) | 1 ligoje |
| SLC2A2solute carrier family 2 member 2 | Dažnai (30–79%) | 2 ligose |
| SLC5A1solute carrier family 5 member 1 | Dažnai (30–79%) | 2 ligose |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Dažnai (30–79%) | 1 ligoje |
| SMOsmoothened, frizzled class receptor | Dažnai (30–79%) | 1 ligoje |
| SMPD1sphingomyelin phosphodiesterase 1 | Dažnai (30–79%) | 2 ligose |
| SREBF1sterol regulatory element binding transcription factor 1 | Dažnai (30–79%) | 1 ligoje |
| TCTN2tectonic family member 2 | Dažnai (30–79%) | 1 ligoje |
| TFAMtranscription factor A, mitochondrial | Dažnai (30–79%) | 1 ligoje |
| TTC7Atetratricopeptide repeat domain 7A | Dažnai (30–79%) | 1 ligoje |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Kartais (5–29%) | 1 ligoje |
| ALADaminolevulinate dehydratase | Kartais (5–29%) | 1 ligoje |
| ALDOBaldolase, fructose-bisphosphate B | Kartais (5–29%) | 1 ligoje |
| ARSAarylsulfatase A | Kartais (5–29%) | 3 ligose |
| CHD8chromodomain helicase DNA binding protein 8 | Kartais (5–29%) | 1 ligoje |
| DDRGK1DDRGK domain containing 1 | Kartais (5–29%) | 2 ligose |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Kartais (5–29%) | 1 ligoje |
| HMBShydroxymethylbilane synthase | Kartais (5–29%) | 1 ligoje |
| IFT56intraflagellar transport 56 | Kartais (5–29%) | 1 ligoje |
| IL12Ainterleukin 12A | Kartais (5–29%) | 1 ligoje |
| IL12RB1interleukin 12 receptor subunit beta 1 | Kartais (5–29%) | 1 ligoje |
| IPO8importin 8 | Kartais (5–29%) | 1 ligoje |
| IRAK1interleukin 1 receptor associated kinase 1 | Kartais (5–29%) | 1 ligoje |
| IRF5interferon regulatory factor 5 | Kartais (5–29%) | 1 ligoje |
| MMEL1membrane metalloendopeptidase like 1 | Kartais (5–29%) | 1 ligoje |
| MPV17mitochondrial inner membrane protein MPV17 | Kartais (5–29%) | 1 ligoje |
| POU2AF1POU class 2 homeobox associating factor 1 | Kartais (5–29%) | 1 ligoje |
| PSAPprosaposin | Kartais (5–29%) | 3 ligose |
| PYGLglycogen phosphorylase L | Kartais (5–29%) | 1 ligoje |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Kartais (5–29%) | 1 ligoje |
| SIsucrase-isomaltase | Kartais (5–29%) | 1 ligoje |
| SPIBSpi-B transcription factor | Kartais (5–29%) | 1 ligoje |
| SPP1secreted phosphoprotein 1 | Kartais (5–29%) | 1 ligoje |
| STAT4signal transducer and activator of transcription 4 | Kartais (5–29%) | 1 ligoje |
| TNFSF15TNF superfamily member 15 | Kartais (5–29%) | 1 ligoje |
| TNPO3transportin 3 | Kartais (5–29%) | 1 ligoje |
| TREHtrehalase | Kartais (5–29%) | 1 ligoje |
| ANK1ankyrin 1 | Retai (1–4 %) | 1 ligoje |
| EPB42erythrocyte membrane protein band 4.2 | Retai (1–4 %) | 1 ligoje |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Retai (1–4 %) | 1 ligoje |
| SPTA1spectrin alpha, erythrocytic 1 | Retai (1–4 %) | 1 ligoje |
| SPTBspectrin beta, erythrocytic | Retai (1–4 %) | 1 ligoje |
| DLL3delta like canonical Notch ligand 3 | Neužfiksuota | 1 ligoje |
| EPHB4EPH receptor B4 | Neužfiksuota | 1 ligoje |
| FLNAfilamin A | Neužfiksuota | 1 ligoje |
| FREM2FRAS1 related extracellular matrix 2 | Neužfiksuota | 1 ligoje |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Neužfiksuota | 1 ligoje |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Neužfiksuota | 1 ligoje |
| KRT18keratin 18 | Neužfiksuota | 1 ligoje |
| MESP2mesoderm posterior bHLH transcription factor 2 | Neužfiksuota | 1 ligoje |
| NPHS1NPHS1 adhesion molecule, nephrin | Neužfiksuota | 1 ligoje |
| SLC26A2solute carrier family 26 member 2 | Neužfiksuota | 1 ligoje |
| SLC26A3solute carrier family 26 member 3 | Neužfiksuota | 1 ligoje |
| SPINT2serine peptidase inhibitor, Kunitz type 2 | Neužfiksuota | 1 ligoje |
| ZEB2zinc finger E-box binding homeobox 2 | 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.
Siauresni požymiai
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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.
AtlasKam padedameMūsų mokslasProduktaiRezultatai
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