AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Požymis
Scar tissue replaces healthy tissue in the liver
Klinikinis pavadinimas: 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.
Santrauka
- Taip pat vadinama
- Hepatic cirrhosis
- Kūno sistema
- Abnormality of the digestive system
AtlasKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
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page$trait$nameKam mes padedameMūsų mokslasProduktaiRezultatai
PrisijungtiKlaustiSekvenuokite savo genomą↗
Vienu tyrimu sužinokite genus, susijusius su Scar tissue replaces healthy tissue in the liver, ir kitą jūsų genomo dalį.
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Įsigyti savo 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 →
Vienu tyrimu sužinokite genus, susijusius su Scar tissue replaces healthy tissue in the liver, ir kitą jūsų genomo dalį.
Nuo 449 $Nemokamas pristatymas · Rezultatai per 6–8 savaites
Įsigyti savo Genome Test152 genų susiję su Scar tissue replaces healthy tissue in the liver
Šių genų pakitimai sukelia retas ligas, kuriose pasireiškia Scar tissue replaces healthy tissue in the liver. 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 |
|---|---|---|
| ABCB11ATP binding cassette subfamily B member 11 | Visada | 2 ligose |
| ABCB4ATP binding cassette subfamily B member 4 | Visada | 1 ligoje |
| ARID2AT-rich interaction domain 2 | Visada | 1 ligoje |
| ATP7BATPase copper transporting beta | Visada | 2 ligose |
| ATP8B1ATPase phospholipid transporting 8B1 | Visada | 2 ligose |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Visada | 2 ligose |
| DHCR77-dehydrocholesterol reductase | Visada | 1 ligoje |
| HAMPhepcidin antimicrobial peptide | Visada | 1 ligoje |
| MPImannose phosphate isomerase | Visada | 1 ligoje |
| NPHP3nephrocystin 3 | Visada | 2 ligose |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Visada | 1 ligoje |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Visada | 2 ligose |
| PSKH1protein serine kinase H1 | Visada | 1 ligoje |
| SERPINA1serpin family A member 1 | Visada | 3 ligose |
| TJP2tight junction protein 2 | Visada | 1 ligoje |
| TRMT5tRNA methyltransferase 5 | Visada | 1 ligoje |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Labai dažnai (80–99%) | 1 ligoje |
| IL12Ainterleukin 12A | Labai dažnai (80–99%) | 1 ligoje |
| IL12RB1interleukin 12 receptor subunit beta 1 | Labai dažnai (80–99%) | 1 ligoje |
| IRF5interferon regulatory factor 5 | Labai dažnai (80–99%) | 1 ligoje |
| MMEL1membrane metalloendopeptidase like 1 | Labai dažnai (80–99%) | 1 ligoje |
| POU2AF1POU class 2 homeobox associating factor 1 | Labai dažnai (80–99%) | 1 ligoje |
| SLC30A10solute carrier family 30 member 10 | Labai dažnai (80–99%) | 1 ligoje |
| SPIBSpi-B transcription factor | Labai dažnai (80–99%) | 1 ligoje |
| TALDO1transaldolase 1 | Labai dažnai (80–99%) | 2 ligose |
| TNFSF15TNF superfamily member 15 | Labai dažnai (80–99%) | 1 ligoje |
| TNPO3transportin 3 | Labai dažnai (80–99%) | 1 ligoje |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Dažnai (30–79%) | 1 ligoje |
| ATP6AP1ATPase H+ transporting accessory protein 1 | Dažnai (30–79%) | 1 ligoje |
| CALRcalreticulin | Dažnai (30–79%) | 1 ligoje |
| COG4component of oligomeric golgi complex 4 | Dažnai (30–79%) | 2 ligose |
| DCDC2doublecortin domain containing 2 | Dažnai (30–79%) | 2 ligose |
| F5coagulation factor V | Dažnai (30–79%) | 2 ligose |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Dažnai (30–79%) | 1 ligoje |
| GPR35G protein-coupled receptor 35 | Dažnai (30–79%) | 1 ligoje |
| HJVhemojuvelin BMP co-receptor | Dažnai (30–79%) | 1 ligoje |
| IFT43intraflagellar transport 43 | Dažnai (30–79%) | 1 ligoje |
| JAK2Janus kinase 2 | Dažnai (30–79%) | 2 ligose |
| KIF12kinesin family member 12 | Dažnai (30–79%) | 1 ligoje |
| KRT18keratin 18 | Dažnai (30–79%) | 1 ligoje |
Rodyti dar 112 genų
| Genas | Kaip dažnai pasireiškia | Ligos |
|---|---|---|
| LIPAlipase A, lysosomal acid type | Dažnai (30–79%) | 2 ligose |
| MPV17mitochondrial inner membrane protein MPV17 | Dažnai (30–79%) | 1 ligoje |
| MST1macrophage stimulating 1 | Dažnai (30–79%) | 1 ligoje |
| NHP2NHP2 ribonucleoprotein | Dažnai (30–79%) | 2 ligose |
| PSMB9proteasome 20S subunit beta 9 | Dažnai (30–79%) | 1 ligoje |
| SEMA4Dsemaphorin 4D | Dažnai (30–79%) | 1 ligoje |
| SKIC2SKI2 subunit of superkiller complex | Dažnai (30–79%) | 2 ligose |
| SKIC3SKI3 subunit of superkiller complex | Dažnai (30–79%) | 2 ligose |
| SLC7A7solute carrier family 7 member 7 | Dažnai (30–79%) | 1 ligoje |
| TCF4transcription factor 4 | Dažnai (30–79%) | 1 ligoje |
| TFAMtranscription factor A, mitochondrial | Dažnai (30–79%) | 1 ligoje |
| TULP3TUB like protein 3 | Dažnai (30–79%) | 1 ligoje |
| YARS1tyrosyl-tRNA synthetase 1 | Dažnai (30–79%) | 1 ligoje |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Kartais (5–29%) | 1 ligoje |
| ACVRL1activin A receptor like type 1 | Kartais (5–29%) | 2 ligose |
| ALMS1ALMS1 centrosome and basal body associated protein | Kartais (5–29%) | 1 ligoje |
| ARHGAP31Rho GTPase activating protein 31 | Kartais (5–29%) | 1 ligoje |
| ASLargininosuccinate lyase | Kartais (5–29%) | 1 ligoje |
| BMP6bone morphogenetic protein 6 | Kartais (5–29%) | 1 ligoje |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Kartais (5–29%) | 2 ligose |
| CC2D2Acoiled-coil and C2 domain containing 2A | Kartais (5–29%) | 1 ligoje |
| CD40LGCD40 ligand | Kartais (5–29%) | 1 ligoje |
| COG6component of oligomeric golgi complex 6 | Kartais (5–29%) | 1 ligoje |
| CTC1CST telomere replication complex component 1 | Kartais (5–29%) | 1 ligoje |
| DKC1dyskerin pseudouridine synthase 1 | Kartais (5–29%) | 2 ligose |
| DLL4delta like canonical Notch ligand 4 | Kartais (5–29%) | 1 ligoje |
| DOCK6dedicator of cytokinesis 6 | Kartais (5–29%) | 1 ligoje |
| ENGendoglin | Kartais (5–29%) | 2 ligose |
| EOGTEGF domain specific O-linked N-acetylglucosamine transferase | Kartais (5–29%) | 1 ligoje |
| FECHferrochelatase | Kartais (5–29%) | 1 ligoje |
| GDF2growth differentiation factor 2 | Kartais (5–29%) | 1 ligoje |
| GLRX5glutaredoxin 5 | Kartais (5–29%) | 1 ligoje |
| HBBhemoglobin subunit beta | Kartais (5–29%) | 3 ligose |
| HFEhomeostatic iron regulator | Kartais (5–29%) | 3 ligose |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Kartais (5–29%) | 2 ligose |
| IFT56intraflagellar transport 56 | Kartais (5–29%) | 1 ligoje |
| IL21Rinterleukin 21 receptor | Kartais (5–29%) | 1 ligoje |
| INPP5Einositol polyphosphate-5-phosphatase E | Kartais (5–29%) | 1 ligoje |
| ITCHitchy E3 ubiquitin protein ligase | Kartais (5–29%) | 1 ligoje |
| LBRlamin B receptor | Kartais (5–29%) | 1 ligoje |
| LIG3DNA ligase 3 | Kartais (5–29%) | 1 ligoje |
| MARS1methionyl-tRNA synthetase 1 | Kartais (5–29%) | 1 ligoje |
| MED12mediator complex subunit 12 | Kartais (5–29%) | 1 ligoje |
| NEK8NIMA related kinase 8 | Kartais (5–29%) | 1 ligoje |
| NOP10NOP10 ribonucleoprotein | Kartais (5–29%) | 1 ligoje |
| NOTCH1notch receptor 1 | Kartais (5–29%) | 1 ligoje |
| NPM1nucleophosmin 1 | Kartais (5–29%) | 1 ligoje |
| PARNpoly(A)-specific ribonuclease | Kartais (5–29%) | 1 ligoje |
| PHKBphosphorylase kinase regulatory subunit beta | Kartais (5–29%) | 1 ligoje |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Kartais (5–29%) | 2 ligose |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Kartais (5–29%) | 1 ligoje |
| POLGDNA polymerase gamma, catalytic subunit | Kartais (5–29%) | 1 ligoje |
| RBPJrecombination signal binding protein for immunoglobulin kappa J region | Kartais (5–29%) | 1 ligoje |
| RPGRIP1LRPGRIP1 like | Kartais (5–29%) | 1 ligoje |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Kartais (5–29%) | 1 ligoje |
| RTEL1regulator of telomere elongation helicase 1 | Kartais (5–29%) | 1 ligoje |
| SLC40A1solute carrier family 40 member 1 | Kartais (5–29%) | 1 ligoje |
| SMAD4SMAD family member 4 | Kartais (5–29%) | 1 ligoje |
| TERCtelomerase RNA component | Kartais (5–29%) | 4 ligose |
| TERTtelomerase reverse transcriptase | Kartais (5–29%) | 4 ligose |
| TFR2transferrin receptor 2 | Kartais (5–29%) | 2 ligose |
| TINF2TERF1 interacting nuclear factor 2 | Kartais (5–29%) | 2 ligose |
| TMEM67transmembrane protein 67 | Kartais (5–29%) | 3 ligose |
| TUBA4Atubulin alpha 4a | Kartais (5–29%) | 1 ligoje |
| TYMPthymidine phosphorylase | Kartais (5–29%) | 1 ligoje |
| TYMSthymidylate synthetase | Kartais (5–29%) | 1 ligoje |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Kartais (5–29%) | 1 ligoje |
| WRAP53WD repeat containing antisense to TP53 | Kartais (5–29%) | 1 ligoje |
| ACBD6acyl-CoA binding domain containing 6 | Retai (1–4 %) | 1 ligoje |
| CEACAM3CEA cell adhesion molecule 3 | Retai (1–4 %) | 1 ligoje |
| CEACAM6CEA cell adhesion molecule 6 | Retai (1–4 %) | 1 ligoje |
| CFTRCF transmembrane conductance regulator | Retai (1–4 %) | 2 ligose |
| CLCA4chloride channel accessory 4 | Retai (1–4 %) | 1 ligoje |
| DCTN4dynactin subunit 4 | Retai (1–4 %) | 1 ligoje |
| EDNRAendothelin receptor type A | Retai (1–4 %) | 1 ligoje |
| FCGR2AFc gamma receptor IIa | Retai (1–4 %) | 1 ligoje |
| GBA1glucosylceramidase beta 1 | Retai (1–4 %) | 1 ligoje |
| GCLCglutamate-cysteine ligase catalytic subunit | Retai (1–4 %) | 1 ligoje |
| GSTM3glutathione S-transferase mu 3 | Retai (1–4 %) | 1 ligoje |
| HMOX1heme oxygenase 1 | Retai (1–4 %) | 1 ligoje |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Retai (1–4 %) | 1 ligoje |
| MIFmacrophage migration inhibitory factor | Retai (1–4 %) | 1 ligoje |
| MTTPmicrosomal triglyceride transfer protein | Retai (1–4 %) | 1 ligoje |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Retai (1–4 %) | 1 ligoje |
| PPARGperoxisome proliferator activated receptor gamma | Retai (1–4 %) | 2 ligose |
| PYGLglycogen phosphorylase L | Retai (1–4 %) | 1 ligoje |
| SCARB2scavenger receptor class B member 2 | Retai (1–4 %) | 1 ligoje |
| SLC11A1solute carrier family 11 member 1 | Retai (1–4 %) | 1 ligoje |
| SLC26A9solute carrier family 26 member 9 | Retai (1–4 %) | 1 ligoje |
| SLC6A14solute carrier family 6 member 14 | Retai (1–4 %) | 1 ligoje |
| SLC9A3solute carrier family 9 member A3 | Retai (1–4 %) | 1 ligoje |
| SMPD1sphingomyelin phosphodiesterase 1 | Retai (1–4 %) | 1 ligoje |
| STX1Asyntaxin 1A | Retai (1–4 %) | 1 ligoje |
| TGFB1transforming growth factor beta 1 | Retai (1–4 %) | 2 ligose |
| AGPAT21-acylglycerol-3-phosphate O-acyltransferase 2 | Neužfiksuota | 1 ligoje |
| ALDOBaldolase, fructose-bisphosphate B | Neužfiksuota | 1 ligoje |
| AP1B1adaptor related protein complex 1 subunit beta 1 | Neužfiksuota | 1 ligoje |
| APOEapolipoprotein E | Neužfiksuota | 1 ligoje |
| ASS1argininosuccinate synthase 1 | Neužfiksuota | 1 ligoje |
| BMP2bone morphogenetic protein 2 | Neužfiksuota | 1 ligoje |
| CPceruloplasmin | Neužfiksuota | 1 ligoje |
| FAHfumarylacetoacetate hydrolase | Neužfiksuota | 1 ligoje |
| GALTgalactose-1-phosphate uridylyltransferase | Neužfiksuota | 1 ligoje |
| GBE11,4-alpha-glucan branching enzyme 1 | Neužfiksuota | 1 ligoje |
| JAG1jagged canonical Notch ligand 1 | Neužfiksuota | 1 ligoje |
| MUC5Bmucin 5B, oligomeric mucus/gel-forming | Neužfiksuota | 1 ligoje |
| PEX1peroxisomal biogenesis factor 1 | Neužfiksuota | 1 ligoje |
| SFTPA2surfactant protein A2 | Neužfiksuota | 1 ligoje |
| SFTPCsurfactant protein C | Neužfiksuota | 1 ligoje |
| SLC25A13solute carrier family 25 member 13 | Neužfiksuota | 1 ligoje |
| URODuroporphyrinogen decarboxylase | Neužfiksuota | 1 ligoje |
| VMA22vacuolar ATPase assembly factor VMA22 | 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.
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- 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.
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