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Cecha
Scar tissue replaces healthy tissue in the liver
Nazwa kliniczna: Cirrhosis
A chronic disorder of the liver in which liver tissue becomes scarred and is partially replaced by regenerative nodules and fibrotic tissue resulting in loss of liver function.
Podsumowanie
- Znana także jako
- Hepatic cirrhosis
- Układ organizmu
- Abnormality of the digestive system
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Ta strona jako dane
Aby odczytać ją jako JSON, dodaj .json na końcu adresu strony lub zażądaj application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/cirrhosis.json"
page <- fromJSON(url)
page$trait$nameKomu pomagamyNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Scar tissue replaces healthy tissue in the liver oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test92 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 12 of these genesNHP2ACDCTC1DKC1NOP10NPM1About this report →
- Adams-Oliver SyndromeReads 6 of these genesARHGAP31DLL4DOCK6EOGTNOTCH1RBPJAbout this report →
- Familial Intrahepatic CholestasisReads 7 of these genesABCB11ABCB4ATP8B1NR1H4PSKH1TJP2About this report →
- HemochromatosisReads 5 of these genesHAMPHJVHFESLC40A1TFR2About this report →
Show 88 more reports
- Hereditary Hemorrhagic TelangiectasiaReads 4 of these genesACVRL1ENGGDF2SMAD4About this report →
- CitrullinemiaReads 2 of these genesASS1SLC25A13About this report →
- Familial Pulmonary FibrosisReads 4 of these genesPARNRTEL1TERTSFTPA2About this report →
- Glycogen Storage DiseaseReads 5 of these genesPHKG2PHKBPHKA2PYGLGBE1About this report →
- Urea Cycle DisorderReads 4 of these genesSLC7A7ASLASS1SLC25A13About this report →
- Disorder of Copper MetabolismReads 2 of these genesATP7BAP1S1About this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Alpha-1 Antitrypsin DeficiencyReads 1 of these genesSERPINA1About this report →
- Björnstad SyndromeReads 1 of these genesBCS1LAbout this report →
- Congenital Bile Acid Synthesis Defect 1 (HSD3B7)Reads 1 of these genesHSD3B7About this report →
- CYP7B1-Related Spastic Paraplegia and Liver DiseaseReads 1 of these genesCYP7B1About this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Hereditary Thrombocythaemia (JAK2)Reads 1 of these genesJAK2About this report →
- ITCH DeficiencyReads 1 of these genesITCHAbout this report →
- Low phospholipid-associated cholelithiasisReads 1 of these genesABCB4About this report →
- Lysosomal Acid Lipase Deficiency (Wolman Disease and CESD)Reads 1 of these genesLIPAAbout this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- Saul-Wilson SyndromeReads 1 of these genesCOG4About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 4 of these genesNPHP3DCDC2NEK8TMEM67About this report →
- LipodystrophyReads 3 of these genesBSCL2PPARGAGPAT2About this report →
- Surfactant Metabolism DysfunctionReads 2 of these genesMARS1SFTPCAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 12 of these genesMPV17YARS1BSCL2LIG3MARS1POLGAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesTERCTERTAbout this report →
- Hepatic Porphyria DisordersReads 2 of these genesFECHURODAbout this report →
- Alagille SyndromeReads 1 of these genesJAG1About this report →
- Hereditary Manganese Transporter DisordersReads 1 of these genesSLC30A10About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Primary Mitochondrial DiseaseReads 8 of these genesTRMT5BCS1LMPV17TFAMLIG3POLGAbout this report →
- PorphyriaReads 2 of these genesFECHURODAbout this report →
- Joubert Syndrome And Related DisordersReads 4 of these genesCC2D2AINPP5ERPGRIP1LTMEM67About this report →
- Meckel SyndromeReads 2 of these genesRPGRIP1LTMEM67About this report →
- Congenital Disorders of GlycosylationReads 6 of these genesMPIATP6AP1COG4COG6PIGAVMA22About this report →
- Polycystic Kidney DiseaseReads 2 of these genesNEK8PKHD1About this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesALDOBAbout this report →
- TyrosinemiaReads 1 of these genesFAHAbout this report →
- Charcot-Marie-Tooth DiseaseReads 5 of these genesMPV17YARS1BSCL2MARS1JAG1About this report →
- Inherited Neurodegenerative DisordersReads 10 of these genesCYP7B1BSCL2CC2D2APOLGTMEM67TUBA4AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 3 of these genesPSMB9SKIC2SKIC3About this report →
- GalactosemiaReads 1 of these genesGALTAbout this report →
- Hyper-IgM SyndromesReads 1 of these genesCD40LGAbout this report →
- Inherited Iron Metabolism DisordersReads 1 of these genesCPAbout this report →
- Alzheimer diseaseReads 1 of these genesAPOEAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- ThalassaemiaReads 1 of these genesHBBAbout this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesTGFB1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesCC2D2ATMEM67MTTPAbout this report →
- Lysosomal Storage DiseaseReads 3 of these genesLIPAGBA1SMPD1About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesIFT43About this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesMTTPAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesGLRX5About this report →
- PolycythemiaReads 1 of these genesHBBAbout this report →
- Pyruvate Kinase Deficiency and Other Red Cell Enzyme DisordersReads 1 of these genesGCLCAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesKCNN4About this report →
- Other Inborn Errors of ImmunityReads 5 of these genesATP6AP1SKIC2SKIC3CD40LGIL21RAbout this report →
- ThrombophiliaReads 1 of these genesF5About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12RB1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesCPAbout this report →
- Rare Inherited Coagulation Factor DeficienciesReads 1 of these genesF5About this report →
- Coffin-Siris SyndromeReads 1 of these genesARID2About this report →
- Type I InterferonopathiesReads 1 of these genesPSMB9About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesSLC9A3About this report →
- HyperlipidemiaReads 1 of these genesAPOEAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesNOTCH1About this report →
- Female InfertilityReads 2 of these genesTUBA4AGALTAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX1About this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesCYP7B1BSCL2About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Retinitis PigmentosaReads 2 of these genesIFT43CC2D2AAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesALMS1About this report →
- Syndromic CraniosynostosisReads 1 of these genesIFT43About this report →
- Intellectual DisabilityReads 3 of these genesTCF4MED12SMAD4About this report →
- VitreoretinopathyReads 1 of these genesCTC1About this report →
- Spinal Muscular AtrophyReads 1 of these genesBSCL2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesTUBA4AAbout this report →
- Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTNPO3About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesAP1B1About this report →
- Male InfertilityReads 1 of these genesCFTRAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesPIGASCARB2About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPEX1About this report →
Odczytaj geny powiązane z Scar tissue replaces healthy tissue in the liver oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test152 genów powiązanych z Scar tissue replaces healthy tissue in the liver
Zmiany w tych genach powodują rzadkie choroby, w których występuje Scar tissue replaces healthy tissue in the liver. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| ABCB11ATP binding cassette subfamily B member 11 | Zawsze | W 2 chorobach |
| ABCB4ATP binding cassette subfamily B member 4 | Zawsze | W 1 chorobie |
| ARID2AT-rich interaction domain 2 | Zawsze | W 1 chorobie |
| ATP7BATPase copper transporting beta | Zawsze | W 2 chorobach |
| ATP8B1ATPase phospholipid transporting 8B1 | Zawsze | W 2 chorobach |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Zawsze | W 2 chorobach |
| DHCR77-dehydrocholesterol reductase | Zawsze | W 1 chorobie |
| HAMPhepcidin antimicrobial peptide | Zawsze | W 1 chorobie |
| MPImannose phosphate isomerase | Zawsze | W 1 chorobie |
| NPHP3nephrocystin 3 | Zawsze | W 2 chorobach |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Zawsze | W 1 chorobie |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Zawsze | W 2 chorobach |
| PSKH1protein serine kinase H1 | Zawsze | W 1 chorobie |
| SERPINA1serpin family A member 1 | Zawsze | W 3 chorobach |
| TJP2tight junction protein 2 | Zawsze | W 1 chorobie |
| TRMT5tRNA methyltransferase 5 | Zawsze | W 1 chorobie |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Bardzo często (80–99%) | W 1 chorobie |
| IL12Ainterleukin 12A | Bardzo często (80–99%) | W 1 chorobie |
| IL12RB1interleukin 12 receptor subunit beta 1 | Bardzo często (80–99%) | W 1 chorobie |
| IRF5interferon regulatory factor 5 | Bardzo często (80–99%) | W 1 chorobie |
| MMEL1membrane metalloendopeptidase like 1 | Bardzo często (80–99%) | W 1 chorobie |
| POU2AF1POU class 2 homeobox associating factor 1 | Bardzo często (80–99%) | W 1 chorobie |
| SLC30A10solute carrier family 30 member 10 | Bardzo często (80–99%) | W 1 chorobie |
| SPIBSpi-B transcription factor | Bardzo często (80–99%) | W 1 chorobie |
| TALDO1transaldolase 1 | Bardzo często (80–99%) | W 2 chorobach |
| TNFSF15TNF superfamily member 15 | Bardzo często (80–99%) | W 1 chorobie |
| TNPO3transportin 3 | Bardzo często (80–99%) | W 1 chorobie |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Często (30–79%) | W 1 chorobie |
| ATP6AP1ATPase H+ transporting accessory protein 1 | Często (30–79%) | W 1 chorobie |
| CALRcalreticulin | Często (30–79%) | W 1 chorobie |
| COG4component of oligomeric golgi complex 4 | Często (30–79%) | W 2 chorobach |
| DCDC2doublecortin domain containing 2 | Często (30–79%) | W 2 chorobach |
| F5coagulation factor V | Często (30–79%) | W 2 chorobach |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Często (30–79%) | W 1 chorobie |
| GPR35G protein-coupled receptor 35 | Często (30–79%) | W 1 chorobie |
| HJVhemojuvelin BMP co-receptor | Często (30–79%) | W 1 chorobie |
| IFT43intraflagellar transport 43 | Często (30–79%) | W 1 chorobie |
| JAK2Janus kinase 2 | Często (30–79%) | W 2 chorobach |
| KIF12kinesin family member 12 | Często (30–79%) | W 1 chorobie |
| KRT18keratin 18 | Często (30–79%) | W 1 chorobie |
Pokaż jeszcze 112 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| LIPAlipase A, lysosomal acid type | Często (30–79%) | W 2 chorobach |
| MPV17mitochondrial inner membrane protein MPV17 | Często (30–79%) | W 1 chorobie |
| MST1macrophage stimulating 1 | Często (30–79%) | W 1 chorobie |
| NHP2NHP2 ribonucleoprotein | Często (30–79%) | W 2 chorobach |
| PSMB9proteasome 20S subunit beta 9 | Często (30–79%) | W 1 chorobie |
| SEMA4Dsemaphorin 4D | Często (30–79%) | W 1 chorobie |
| SKIC2SKI2 subunit of superkiller complex | Często (30–79%) | W 2 chorobach |
| SKIC3SKI3 subunit of superkiller complex | Często (30–79%) | W 2 chorobach |
| SLC7A7solute carrier family 7 member 7 | Często (30–79%) | W 1 chorobie |
| TCF4transcription factor 4 | Często (30–79%) | W 1 chorobie |
| TFAMtranscription factor A, mitochondrial | Często (30–79%) | W 1 chorobie |
| TULP3TUB like protein 3 | Często (30–79%) | W 1 chorobie |
| YARS1tyrosyl-tRNA synthetase 1 | Często (30–79%) | W 1 chorobie |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Czasami (5–29%) | W 1 chorobie |
| ACVRL1activin A receptor like type 1 | Czasami (5–29%) | W 2 chorobach |
| ALMS1ALMS1 centrosome and basal body associated protein | Czasami (5–29%) | W 1 chorobie |
| ARHGAP31Rho GTPase activating protein 31 | Czasami (5–29%) | W 1 chorobie |
| ASLargininosuccinate lyase | Czasami (5–29%) | W 1 chorobie |
| BMP6bone morphogenetic protein 6 | Czasami (5–29%) | W 1 chorobie |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Czasami (5–29%) | W 2 chorobach |
| CC2D2Acoiled-coil and C2 domain containing 2A | Czasami (5–29%) | W 1 chorobie |
| CD40LGCD40 ligand | Czasami (5–29%) | W 1 chorobie |
| COG6component of oligomeric golgi complex 6 | Czasami (5–29%) | W 1 chorobie |
| CTC1CST telomere replication complex component 1 | Czasami (5–29%) | W 1 chorobie |
| DKC1dyskerin pseudouridine synthase 1 | Czasami (5–29%) | W 2 chorobach |
| DLL4delta like canonical Notch ligand 4 | Czasami (5–29%) | W 1 chorobie |
| DOCK6dedicator of cytokinesis 6 | Czasami (5–29%) | W 1 chorobie |
| ENGendoglin | Czasami (5–29%) | W 2 chorobach |
| EOGTEGF domain specific O-linked N-acetylglucosamine transferase | Czasami (5–29%) | W 1 chorobie |
| FECHferrochelatase | Czasami (5–29%) | W 1 chorobie |
| GDF2growth differentiation factor 2 | Czasami (5–29%) | W 1 chorobie |
| GLRX5glutaredoxin 5 | Czasami (5–29%) | W 1 chorobie |
| HBBhemoglobin subunit beta | Czasami (5–29%) | W 3 chorobach |
| HFEhomeostatic iron regulator | Czasami (5–29%) | W 3 chorobach |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Czasami (5–29%) | W 2 chorobach |
| IFT56intraflagellar transport 56 | Czasami (5–29%) | W 1 chorobie |
| IL21Rinterleukin 21 receptor | Czasami (5–29%) | W 1 chorobie |
| INPP5Einositol polyphosphate-5-phosphatase E | Czasami (5–29%) | W 1 chorobie |
| ITCHitchy E3 ubiquitin protein ligase | Czasami (5–29%) | W 1 chorobie |
| LBRlamin B receptor | Czasami (5–29%) | W 1 chorobie |
| LIG3DNA ligase 3 | Czasami (5–29%) | W 1 chorobie |
| MARS1methionyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| MED12mediator complex subunit 12 | Czasami (5–29%) | W 1 chorobie |
| NEK8NIMA related kinase 8 | Czasami (5–29%) | W 1 chorobie |
| NOP10NOP10 ribonucleoprotein | Czasami (5–29%) | W 1 chorobie |
| NOTCH1notch receptor 1 | Czasami (5–29%) | W 1 chorobie |
| NPM1nucleophosmin 1 | Czasami (5–29%) | W 1 chorobie |
| PARNpoly(A)-specific ribonuclease | Czasami (5–29%) | W 1 chorobie |
| PHKBphosphorylase kinase regulatory subunit beta | Czasami (5–29%) | W 1 chorobie |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Czasami (5–29%) | W 2 chorobach |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Czasami (5–29%) | W 1 chorobie |
| POLGDNA polymerase gamma, catalytic subunit | Czasami (5–29%) | W 1 chorobie |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Czasami (5–29%) | W 1 chorobie |
| RPGRIP1LRPGRIP1 like | Czasami (5–29%) | W 1 chorobie |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Czasami (5–29%) | W 1 chorobie |
| RTEL1regulator of telomere elongation helicase 1 | Czasami (5–29%) | W 1 chorobie |
| SLC40A1solute carrier family 40 member 1 | Czasami (5–29%) | W 1 chorobie |
| SMAD4SMAD family member 4 | Czasami (5–29%) | W 1 chorobie |
| TERCtelomerase RNA component | Czasami (5–29%) | W 4 chorobach |
| TERTtelomerase reverse transcriptase | Czasami (5–29%) | W 4 chorobach |
| TFR2transferrin receptor 2 | Czasami (5–29%) | W 2 chorobach |
| TINF2TERF1 interacting nuclear factor 2 | Czasami (5–29%) | W 2 chorobach |
| TMEM67transmembrane protein 67 | Czasami (5–29%) | W 3 chorobach |
| TUBA4Atubulin alpha 4a | Czasami (5–29%) | W 1 chorobie |
| TYMPthymidine phosphorylase | Czasami (5–29%) | W 1 chorobie |
| TYMSthymidylate synthetase | Czasami (5–29%) | W 1 chorobie |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Czasami (5–29%) | W 1 chorobie |
| WRAP53WD repeat containing antisense to TP53 | Czasami (5–29%) | W 1 chorobie |
| ACBD6acyl-CoA binding domain containing 6 | Rzadko (1–4%) | W 1 chorobie |
| CEACAM3CEA cell adhesion molecule 3 | Rzadko (1–4%) | W 1 chorobie |
| CEACAM6CEA cell adhesion molecule 6 | Rzadko (1–4%) | W 1 chorobie |
| CFTRCF transmembrane conductance regulator | Rzadko (1–4%) | W 2 chorobach |
| CLCA4chloride channel accessory 4 | Rzadko (1–4%) | W 1 chorobie |
| DCTN4dynactin subunit 4 | Rzadko (1–4%) | W 1 chorobie |
| EDNRAendothelin receptor type A | Rzadko (1–4%) | W 1 chorobie |
| FCGR2AFc gamma receptor IIa | Rzadko (1–4%) | W 1 chorobie |
| GBA1glucosylceramidase beta 1 | Rzadko (1–4%) | W 1 chorobie |
| GCLCglutamate-cysteine ligase catalytic subunit | Rzadko (1–4%) | W 1 chorobie |
| GSTM3glutathione S-transferase mu 3 | Rzadko (1–4%) | W 1 chorobie |
| HMOX1heme oxygenase 1 | Rzadko (1–4%) | W 1 chorobie |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Rzadko (1–4%) | W 1 chorobie |
| MIFmacrophage migration inhibitory factor | Rzadko (1–4%) | W 1 chorobie |
| MTTPmicrosomal triglyceride transfer protein | Rzadko (1–4%) | W 1 chorobie |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Rzadko (1–4%) | W 1 chorobie |
| PPARGperoxisome proliferator activated receptor gamma | Rzadko (1–4%) | W 2 chorobach |
| PYGLglycogen phosphorylase L | Rzadko (1–4%) | W 1 chorobie |
| SCARB2scavenger receptor class B member 2 | Rzadko (1–4%) | W 1 chorobie |
| SLC11A1solute carrier family 11 member 1 | Rzadko (1–4%) | W 1 chorobie |
| SLC26A9solute carrier family 26 member 9 | Rzadko (1–4%) | W 1 chorobie |
| SLC6A14solute carrier family 6 member 14 | Rzadko (1–4%) | W 1 chorobie |
| SLC9A3solute carrier family 9 member A3 | Rzadko (1–4%) | W 1 chorobie |
| SMPD1sphingomyelin phosphodiesterase 1 | Rzadko (1–4%) | W 1 chorobie |
| STX1Asyntaxin 1A | Rzadko (1–4%) | W 1 chorobie |
| TGFB1transforming growth factor beta 1 | Rzadko (1–4%) | W 2 chorobach |
| AGPAT21-acylglycerol-3-phosphate O-acyltransferase 2 | Nie odnotowano | W 1 chorobie |
| ALDOBaldolase, fructose-bisphosphate B | Nie odnotowano | W 1 chorobie |
| AP1B1adaptor related protein complex 1 subunit beta 1 | Nie odnotowano | W 1 chorobie |
| APOEapolipoprotein E | Nie odnotowano | W 1 chorobie |
| ASS1argininosuccinate synthase 1 | Nie odnotowano | W 1 chorobie |
| BMP2bone morphogenetic protein 2 | Nie odnotowano | W 1 chorobie |
| CPceruloplasmin | Nie odnotowano | W 1 chorobie |
| FAHfumarylacetoacetate hydrolase | Nie odnotowano | W 1 chorobie |
| GALTgalactose-1-phosphate uridylyltransferase | Nie odnotowano | W 1 chorobie |
| GBE11,4-alpha-glucan branching enzyme 1 | Nie odnotowano | W 1 chorobie |
| JAG1jagged canonical Notch ligand 1 | Nie odnotowano | W 1 chorobie |
| MUC5Bmucin 5B, oligomeric mucus/gel-forming | Nie odnotowano | W 1 chorobie |
| PEX1peroxisomal biogenesis factor 1 | Nie odnotowano | W 1 chorobie |
| SFTPA2surfactant protein A2 | Nie odnotowano | W 1 chorobie |
| SFTPCsurfactant protein C | Nie odnotowano | W 1 chorobie |
| SLC25A13solute carrier family 25 member 13 | Nie odnotowano | W 1 chorobie |
| URODuroporphyrinogen decarboxylase | Nie odnotowano | W 1 chorobie |
| VMA22vacuolar ATPase assembly factor VMA22 | Nie odnotowano | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy podrzędne
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.19-9814e911.
AtlasKomu pomagamyNasza naukaProduktyWyniki
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