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Egenskap
Diarrhea
Abnormally increased frequency (usually defined as three or more) loose or watery bowel movements a day.
Sammendrag
- Også kalt
- Watery stool, Diarrhoea
- Kroppssystem
- Abnormality of the digestive system
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/diarrhea.json"
page <- fromJSON(url)
page$trait$nameDiarrheaHP:0002014
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Les genene knyttet til Diarrhea, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test146 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.
- Other Inborn Errors of ImmunityReads 55 of these genesADAAK2CD79ACD79BIL2RBIRF4About this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 9 of these genesCD79ACD79BBLNKIGHMIGLL1PIK3R1About this report →
- Severe Combined ImmunodeficiencyReads 16 of these genesADAAK2LCKCIITAIL2RGRFX5About this report →
- Parkinson DiseaseReads 8 of these genesDNAJC6LRRK2PARK7PINK1PRKNSNCAAbout this report →
Show 142 more reports
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 4 of these genesSGSHGNSHGSNATNAGLUAbout this report →
- Congenital Diarrhoeas & EnteropathiesReads 7 of these genesDGAT1WNT2BNEUROG3SLC5A1MYO5BSTX3About this report →
- Familial Glucocorticoid DeficiencyReads 5 of these genesMC2RMRAPNNTNR0B1TXNRD2About this report →
- Malignant Endocrine NeoplasmReads 5 of these genesSDHASDHBCDKN1BMEN1RETAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 7 of these genesCPT1AHMGCS2HADHCPT2ACADMHMGCLAbout this report →
- Autoimmune DiseaseReads 8 of these genesAIRECTLA4NOD2STAT1DNASE1L3STAT3About this report →
- Hereditary Optic NeuropathyReads 6 of these genesDNM1LATP1A3MT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 5 of these genesIKZF1CD19CR2ICOSTNFRSF13BAbout this report →
- Familial Intrahepatic CholestasisReads 5 of these genesABCB11ABCB4ATP8B1MYO5BZFYVE19About this report →
- Hereditary Episodic AtaxiasReads 3 of these genesCACNA1ASCN2ASLC1A3About this report →
- Lysosomal Storage DiseaseReads 11 of these genesSGSHLIPAHEXBSMPD1AGACYP27A1About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
- Congenital Disaccharidase DeficienciesReads 2 of these genesSILCTAbout this report →
- Juvenile Polyposis SyndromeReads 2 of these genesBMPR1ASMAD4About this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 2 of these genesSTAT1STAT3About this report →
- Bartter DiseaseReads 3 of these genesCLCNKBKCNJ1SLC12A1About this report →
- Congenital Disorders of GlycosylationReads 13 of these genesALG8CADMPIPIGTALG2COG7About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 4 of these genesSDHASDHBSDHCRETAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 7 of these genesLYNOTULINSKIC2ELF4DOCK11IFIH1About this report →
- Severe Congenital NeutropeniaReads 4 of these genesCLPBELANEGFI1WASAbout this report →
- Urea Cycle DisorderReads 4 of these genesSLC25A13SLC7A7ASLNAGSAbout this report →
- Disorder of Copper MetabolismReads 2 of these genesAP1S1ATP7AAbout this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 2 of these genesALDOBFBP1About this report →
- Rothmund-Thomson SyndromeReads 2 of these genesRECQL4ANAPC1About this report →
- Classic Organic AciduriasReads 3 of these genesACAT1HMGCLMLYCDAbout this report →
- Hepatic Porphyria DisordersReads 3 of these genesALADHMBSCPOXAbout this report →
- Glycogen Storage DiseaseReads 4 of these genesSLC37A4PHKA2PHKBPHKG2About this report →
- PorphyriaReads 3 of these genesALADHMBSCPOXAbout this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- Cerebrotendinous XanthomatosisReads 1 of these genesCYP27A1About this report →
- CHAPLE Disease (CD55 Deficiency)Reads 1 of these genesCD55About this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout 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 →
- Glucose-Galactose MalabsorptionReads 1 of these genesSLC5A1About this report →
- Hepatic Veno-Occlusive Disease with Immunodeficiency (VODI)Reads 1 of these genesSP110About this report →
- Hereditary Folate MalabsorptionReads 1 of these genesSLC46A1About 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 →
- Mucopolysaccharidosis Type II (Hunter Syndrome)Reads 1 of these genesIDSAbout this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 3 of these genesSTAT1IFNGR1IL23RAbout this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 3 of these genesDDCDBHMAOAAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 4 of these genesNGFELP1SCN11ASCN9AAbout this report →
- Urinary and Renal System TumourReads 3 of these genesSDHASDHBRETAbout this report →
- Leigh SyndromeReads 7 of these genesSDHAETHE1MT-ND1MT-ND4MT-ND5MT-ND6About this report →
- Hereditary Periodic Fever SyndromesReads 2 of these genesMVKTNFRSF1AAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 2 of these genesERBB3ACTG2About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 2 of these genesKCNK3CAV1About this report →
- Inflammatory Bowel Diseases (IBD)Reads 2 of these genesTGFB1IL10About this report →
- Systemic Lupus ErythematosusReads 2 of these genesDNASE1L3SAT1About this report →
- DNA Repair DiseaseReads 5 of these genesERCC4ERCC6ERCC8DCLRE1CNBNAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 2 of these genesCTLA4FASAbout this report →
- Hereditary HypolipoproteinemiasReads 2 of these genesAPOA1SAR1BAbout this report →
- IPEX Syndrome and Other TregopathiesReads 2 of these genesIL2RBCTLA4About this report →
- Waardenburg SyndromeReads 2 of these genesEDN3EDNRBAbout this report →
- Epilepsy (Full Panel)Reads 10 of these genesCADATP1A2ATP1A3CACNA1ARHOBTB2SCN2AAbout this report →
- Diabetes MellitusReads 4 of these genesNEUROG3HNF4AMT-TL1RFX6About this report →
- Thyroid CancerReads 4 of these genesTSHRAIREMEN1RETAbout this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Biotinidase & Holocarboxylase DeficiencyReads 1 of these genesBTDAbout this report →
- CitrullinemiaReads 1 of these genesSLC25A13About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Hereditary FibromatosesReads 1 of these genesANTXR2About this report →
- Myotonic DystrophyReads 1 of these genesDMPKAbout this report →
- Sandhoff Disease and GM2 Activator DeficiencyReads 1 of these genesHEXBAbout this report →
- Shwachman-Diamond SyndromeReads 1 of these genesEFL1About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Homocystinuria & Cobalamin DisordersReads 3 of these genesMTRTCN2AMNAbout this report →
- HyperinsulinismReads 2 of these genesHADHPMM2About this report →
- Polycystic Kidney DiseaseReads 2 of these genesALG8ALG9About this report →
- Hereditary AmyloidosisReads 2 of these genesAPOA1TTRAbout this report →
- Hereditary AngioedemaReads 1 of these genesSERPING1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesRETAbout this report →
- HyperthyroidismReads 1 of these genesTSHRAbout this report →
- MedulloblastomaReads 1 of these genesELP1About this report →
- Methylmalonic & Propionic AcidemiaReads 2 of these genesMMUTACSF3About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 2 of these genesNR3C2SCNN1AAbout this report →
- Primary Mitochondrial DiseaseReads 6 of these genesPOLGTYMPLIG3MPV17RRM2BMGME1About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- GalactosemiaReads 1 of these genesGALTAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Hyper-IgM SyndromesReads 1 of these genesCD40LGAbout this report →
- Polycystic Liver Disease (1 and 2)Reads 1 of these genesALG8About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Thiamine Transporter and Metabolism DisordersReads 1 of these genesSLC19A2About this report →
- Intellectual DisabilityReads 7 of these genesKDM6BASXL1SCN2ASMAD4CHD8NAA10About this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesITPR3MPV17ATP7ANAGLUAbout this report →
- Chronic Mucocutaneous CandidiasisReads 1 of these genesSTAT1About 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 →
- Dyskeratosis CongenitaReads 2 of these genesZBTB24DNMT3BAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesRECQL4SMOAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF4About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesAGAAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAPCAbout this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesSTARAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 1 of these genesPCSK1About this report →
- Hereditary Spastic ParaplegiaReads 3 of these genesABCD1UCHL1CYP7B1About this report →
- Aicardi-Goutieres SyndromeReads 1 of these genesIFIH1About this report →
- PolycythemiaReads 1 of these genesHBBAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesDESAbout this report →
- Inherited ThrombocytopeniasReads 2 of these genesRUNX1WASAbout this report →
- Other Inherited LeukodystrophiesReads 3 of these genesABCD1IFIH1CYP27A1About 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 →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 1 of these genesCFHAbout this report →
- Kidney CancerReads 1 of these genesSDHBAbout this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesDESAbout this report →
- LipodystrophyReads 1 of these genesCAV1About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF4AAbout this report →
- Type I InterferonopathiesReads 1 of these genesIFIH1About this report →
- Dilated CardiomyopathyReads 2 of these genesDOLKDESAbout this report →
- Hypogonadotropic HypogonadismReads 2 of these genesNR0B1PCSK1About this report →
- Myofibrillar MyopathiesReads 1 of these genesDESAbout this report →
- Female InfertilityReads 2 of these genesSTARGALTAbout this report →
- OsteopetrosisReads 1 of these genesTCIRG1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 2 of these genesRNF168CYP27A1About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC4AAbout this report →
- Fanconi AnemiaReads 1 of these genesERCC4About this report →
- Congenital HypothyroidismReads 1 of these genesTSHRAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGTAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesNEUROG3About this report →
- Noonan SyndromeReads 1 of these genesCBLAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesALG2About this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Nephrotic SyndromeReads 1 of these genesPODXLAbout this report →
- Osteogenesis ImperfectaReads 1 of these genesIFIH1About this report →
- Male InfertilityReads 1 of these genesCFTRAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesDMPKAbout this report →
- Retinitis PigmentosaReads 1 of these genesHGSNATAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesKARS1About this report →
Les genene knyttet til Diarrhea, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test316 gener knyttet til Diarrhea
Endringer i disse genene forårsaker sjeldne tilstander der Diarrhea forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ABCB11ATP binding cassette subfamily B member 11 | Alltid | I 2 tilstander |
| ABCB4ATP binding cassette subfamily B member 4 | Alltid | I 1 tilstand |
| ADAadenosine deaminase | Alltid | I 2 tilstander |
| AK2adenylate kinase 2 | Alltid | I 2 tilstander |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Alltid | I 2 tilstander |
| ANO1anoctamin 1 | Alltid | I 1 tilstand |
| AP1S1adaptor related protein complex 1 subunit sigma 1 | Alltid | I 1 tilstand |
| APOA1apolipoprotein A1 | Alltid | I 1 tilstand |
| ATP8B1ATPase phospholipid transporting 8B1 | Alltid | I 2 tilstander |
| CADcarbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase | Alltid | I 1 tilstand |
| CD79ACD79a molecule | Alltid | I 2 tilstander |
| CD79BCD79b molecule | Alltid | I 2 tilstander |
| CPT1Acarnitine palmitoyltransferase 1A | Alltid | I 1 tilstand |
| DGAT1diacylglycerol O-acyltransferase 1 | Alltid | I 1 tilstand |
| DNM1Ldynamin 1L | Alltid | I 1 tilstand |
| DOT1LDOT1 like histone lysine methyltransferase | Alltid | I 1 tilstand |
| FEM1Bfem-1 homolog B | Alltid | I 1 tilstand |
| GRWD1glutamate rich WD repeat containing 1 | Alltid | I 1 tilstand |
| HMGCS23-hydroxy-3-methylglutaryl-CoA synthase 2 | Alltid | I 1 tilstand |
| IL2RBinterleukin 2 receptor subunit beta | Alltid | I 1 tilstand |
| IRF4interferon regulatory factor 4 | Alltid | I 2 tilstander |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Alltid | I 1 tilstand |
| KCNK3potassium two pore domain channel subfamily K member 3 | Alltid | I 1 tilstand |
| KDM6Blysine demethylase 6B | Alltid | I 1 tilstand |
| LCKLCK proto-oncogene, Src family tyrosine kinase | Alltid | I 1 tilstand |
| LYNLYN proto-oncogene, Src family tyrosine kinase | Alltid | I 1 tilstand |
| MCM10minichromosome maintenance 10 replication initiation factor | Alltid | I 1 tilstand |
| MPImannose phosphate isomerase | Alltid | I 2 tilstander |
| MYO1Amyosin IA | Alltid | I 1 tilstand |
| NCF4neutrophil cytosolic factor 4 | Alltid | I 1 tilstand |
| OTULINOTU deubiquitinase with linear linkage specificity | Alltid | I 1 tilstand |
| PERCC1proline and glutamate rich with coiled coil 1 | Alltid | I 1 tilstand |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Alltid | I 1 tilstand |
| PIK3CGphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | Alltid | I 1 tilstand |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Alltid | I 1 tilstand |
| RIPK1receptor interacting serine/threonine kinase 1 | Alltid | I 1 tilstand |
| RNU6ATACRNA, U6atac small nuclear | Alltid | I 1 tilstand |
| SAR1Bsecretion associated Ras related GTPase 1B | Alltid | I 2 tilstander |
| SGSM3small G protein signaling modulator 3 | Alltid | I 1 tilstand |
| SIsucrase-isomaltase | Alltid | I 2 tilstander |
Vis 276 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| SKIC2SKI2 subunit of superkiller complex | Alltid | I 1 tilstand |
| SLC46A1solute carrier family 46 member 1 | Alltid | I 2 tilstander |
| TRACT cell receptor alpha constant | Alltid | I 1 tilstand |
| WNT2BWnt family member 2B | Alltid | I 1 tilstand |
| BLNKB cell linker | Svært ofte (80–99 %) | I 1 tilstand |
| BMPR1Abone morphogenetic protein receptor type 1A | Svært ofte (80–99 %) | I 2 tilstander |
| CD4CD4 molecule | Svært ofte (80–99 %) | I 1 tilstand |
| EFL1elongation factor like GTPase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| HADHhydroxyacyl-CoA dehydrogenase | Svært ofte (80–99 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Svært ofte (80–99 %) | I 3 tilstander |
| IGHMimmunoglobulin heavy constant mu | Svært ofte (80–99 %) | I 1 tilstand |
| IGLL1immunoglobulin lambda like polypeptide 1 | Svært ofte (80–99 %) | I 1 tilstand |
| IKZF1IKAROS family zinc finger 1 | Svært ofte (80–99 %) | I 1 tilstand |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Svært ofte (80–99 %) | I 1 tilstand |
| MVKmevalonate kinase | Svært ofte (80–99 %) | I 3 tilstander |
| NEUROG3neurogenin 3 | Svært ofte (80–99 %) | I 2 tilstander |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Svært ofte (80–99 %) | I 3 tilstander |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Svært ofte (80–99 %) | I 2 tilstander |
| POLGDNA polymerase gamma, catalytic subunit | Svært ofte (80–99 %) | I 2 tilstander |
| PTENphosphatase and tensin homolog | Svært ofte (80–99 %) | I 1 tilstand |
| RECQL4RecQ like helicase 4 | Svært ofte (80–99 %) | I 3 tilstander |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Svært ofte (80–99 %) | I 1 tilstand |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Svært ofte (80–99 %) | I 1 tilstand |
| SDHCsuccinate dehydrogenase complex subunit C | Svært ofte (80–99 %) | I 1 tilstand |
| SGSHN-sulfoglucosamine sulfohydrolase | Svært ofte (80–99 %) | I 1 tilstand |
| SLC19A2solute carrier family 19 member 2 | Svært ofte (80–99 %) | I 1 tilstand |
| SLC5A1solute carrier family 5 member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| SPI1Spi-1 proto-oncogene | Svært ofte (80–99 %) | I 1 tilstand |
| SYKspleen associated tyrosine kinase | Svært ofte (80–99 %) | I 1 tilstand |
| TCF3transcription factor 3 | Svært ofte (80–99 %) | I 1 tilstand |
| TNFRSF1ATNF receptor superfamily member 1A | Svært ofte (80–99 %) | I 1 tilstand |
| TSHRthyroid stimulating hormone receptor | Svært ofte (80–99 %) | I 2 tilstander |
| TYMPthymidine phosphorylase | Svært ofte (80–99 %) | I 2 tilstander |
| ACAT1acetyl-CoA acetyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| AIREautoimmune regulator | Ofte (30–79 %) | I 1 tilstand |
| ALDOBaldolase, fructose-bisphosphate B | Ofte (30–79 %) | I 1 tilstand |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Ofte (30–79 %) | I 1 tilstand |
| ANTXR2ANTXR cell adhesion molecule 2 | Ofte (30–79 %) | I 1 tilstand |
| APCAPC regulator of Wnt signaling pathway | Ofte (30–79 %) | I 1 tilstand |
| ASXL1ASXL transcriptional regulator 1 | Ofte (30–79 %) | I 2 tilstander |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Ofte (30–79 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Ofte (30–79 %) | I 1 tilstand |
| AVParginine vasopressin | Ofte (30–79 %) | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Ofte (30–79 %) | I 1 tilstand |
| CAV1caveolin 1 | Ofte (30–79 %) | I 1 tilstand |
| CBLCbl proto-oncogene | Ofte (30–79 %) | I 1 tilstand |
| CD40LGCD40 ligand | Ofte (30–79 %) | I 1 tilstand |
| CD55CD55 molecule (Cromer blood group) | Ofte (30–79 %) | I 1 tilstand |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Ofte (30–79 %) | I 2 tilstander |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Ofte (30–79 %) | I 1 tilstand |
| CIITAclass II major histocompatibility complex transactivator | Ofte (30–79 %) | I 1 tilstand |
| CLPBClpB family mitochondrial disaggregase | Ofte (30–79 %) | I 1 tilstand |
| COG7component of oligomeric golgi complex 7 | Ofte (30–79 %) | I 1 tilstand |
| CPT2carnitine palmitoyltransferase 2 | Ofte (30–79 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Ofte (30–79 %) | I 2 tilstander |
| DDCdopa decarboxylase | Ofte (30–79 %) | I 2 tilstander |
| ELANEelastase, neutrophil expressed | Ofte (30–79 %) | I 1 tilstand |
| ELF4E74 like ETS transcription factor 4 | Ofte (30–79 %) | I 1 tilstand |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ofte (30–79 %) | I 1 tilstand |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Ofte (30–79 %) | I 1 tilstand |
| ETHE1ETHE1 persulfide dioxygenase | Ofte (30–79 %) | I 1 tilstand |
| FBP1fructose-bisphosphatase 1 | Ofte (30–79 %) | I 1 tilstand |
| FOCADfocadhesin | Ofte (30–79 %) | I 1 tilstand |
| GFI1growth factor independent 1 transcriptional repressor | Ofte (30–79 %) | I 1 tilstand |
| GINS1GINS complex subunit 1 | Ofte (30–79 %) | I 1 tilstand |
| HNF4Ahepatocyte nuclear factor 4 alpha | Ofte (30–79 %) | I 1 tilstand |
| HPGD15-hydroxyprostaglandin dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| IL2RGinterleukin 2 receptor subunit gamma | Ofte (30–79 %) | I 1 tilstand |
| IRF1interferon regulatory factor 1 | Ofte (30–79 %) | I 1 tilstand |
| KITKIT proto-oncogene, receptor tyrosine kinase | Ofte (30–79 %) | I 2 tilstander |
| LIG3DNA ligase 3 | Ofte (30–79 %) | I 1 tilstand |
| LIPAlipase A, lysosomal acid type | Ofte (30–79 %) | I 2 tilstander |
| MC2Rmelanocortin 2 receptor | Ofte (30–79 %) | I 1 tilstand |
| MEFVMEFV innate immunity regulator, pyrin | Ofte (30–79 %) | I 3 tilstander |
| MEN1menin 1 | Ofte (30–79 %) | I 2 tilstander |
| MPV17mitochondrial inner membrane protein MPV17 | Ofte (30–79 %) | I 1 tilstand |
| MRAPmelanocortin 2 receptor accessory protein | Ofte (30–79 %) | I 1 tilstand |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Ofte (30–79 %) | I 1 tilstand |
| MTR5-methyltetrahydrofolate-homocysteine methyltransferase | Ofte (30–79 %) | I 1 tilstand |
| MYO5Bmyosin VB | Ofte (30–79 %) | I 1 tilstand |
| NGFnerve growth factor | Ofte (30–79 %) | I 1 tilstand |
| NNTnicotinamide nucleotide transhydrogenase | Ofte (30–79 %) | I 1 tilstand |
| NOD2nucleotide binding oligomerization domain containing 2 | Ofte (30–79 %) | I 2 tilstander |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Ofte (30–79 %) | I 1 tilstand |
| RFX5regulatory factor X5 | Ofte (30–79 %) | I 1 tilstand |
| RFXANKregulatory factor X associated ankyrin containing protein | Ofte (30–79 %) | I 1 tilstand |
| RFXAPregulatory factor X associated protein | Ofte (30–79 %) | I 1 tilstand |
| RHOBTB2Rho related BTB domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Ofte (30–79 %) | I 2 tilstander |
| RUNX1RUNX family transcription factor 1 | Ofte (30–79 %) | I 1 tilstand |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| SERPING1serpin family G member 1 | Ofte (30–79 %) | I 2 tilstander |
| SLC1A3solute carrier family 1 member 3 | Ofte (30–79 %) | I 1 tilstand |
| SLC25A13solute carrier family 25 member 13 | Ofte (30–79 %) | I 2 tilstander |
| SLC2A1solute carrier family 2 member 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC39A4solute carrier family 39 member 4 | Ofte (30–79 %) | I 1 tilstand |
| SLC7A7solute carrier family 7 member 7 | Ofte (30–79 %) | I 2 tilstander |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Ofte (30–79 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Ofte (30–79 %) | I 1 tilstand |
| SRP19signal recognition particle 19 | Ofte (30–79 %) | I 1 tilstand |
| SRSF2serine and arginine rich splicing factor 2 | Ofte (30–79 %) | I 2 tilstander |
| STARsteroidogenic acute regulatory protein | Ofte (30–79 %) | I 1 tilstand |
| STAT1signal transducer and activator of transcription 1 | Ofte (30–79 %) | I 2 tilstander |
| STX3syntaxin 3 | Ofte (30–79 %) | I 1 tilstand |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Ofte (30–79 %) | I 1 tilstand |
| TCN2transcobalamin 2 | Ofte (30–79 %) | I 1 tilstand |
| TET2tet methylcytosine dioxygenase 2 | Ofte (30–79 %) | I 2 tilstander |
| TTRtransthyretin | Ofte (30–79 %) | I 2 tilstander |
| TXNRD2thioredoxin reductase 2 | Ofte (30–79 %) | I 1 tilstand |
| UQCRHubiquinol-cytochrome c reductase hinge protein | Ofte (30–79 %) | I 1 tilstand |
| WDR1WD repeat domain 1 | Ofte (30–79 %) | I 1 tilstand |
| ABCD1ATP binding cassette subfamily D member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ACADMacyl-CoA dehydrogenase medium chain | Noen ganger (5–29 %) | I 1 tilstand |
| ALADaminolevulinate dehydratase | Noen ganger (5–29 %) | I 1 tilstand |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Noen ganger (5–29 %) | I 1 tilstand |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| AMNamnion associated transmembrane protein | Noen ganger (5–29 %) | I 1 tilstand |
| ANAPC1anaphase promoting complex subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ASLargininosuccinate lyase | Noen ganger (5–29 %) | I 1 tilstand |
| ATP7AATPase copper transporting alpha | Noen ganger (5–29 %) | I 1 tilstand |
| B4GALT1beta-1,4-galactosyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CD247CD247 molecule | Noen ganger (5–29 %) | I 1 tilstand |
| CD3DCD3 delta subunit of T-cell receptor complex | Noen ganger (5–29 %) | I 1 tilstand |
| CD3ECD3 epsilon subunit of T-cell receptor complex | Noen ganger (5–29 %) | I 1 tilstand |
| CFTRCF transmembrane conductance regulator | Noen ganger (5–29 %) | I 1 tilstand |
| CHD8chromodomain helicase DNA binding protein 8 | Noen ganger (5–29 %) | I 1 tilstand |
| DBHdopamine beta-hydroxylase | Noen ganger (5–29 %) | I 1 tilstand |
| DMPKDM1 protein kinase | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC6DnaJ heat shock protein family (Hsp40) member C6 | Noen ganger (5–29 %) | I 1 tilstand |
| DNASE1L3deoxyribonuclease 1L3 | Noen ganger (5–29 %) | I 1 tilstand |
| DOCK11dedicator of cytokinesis 11 | Noen ganger (5–29 %) | I 1 tilstand |
| DOLKdolichol kinase | Noen ganger (5–29 %) | I 1 tilstand |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Noen ganger (5–29 %) | I 1 tilstand |
| ECE1endothelin converting enzyme 1 | Noen ganger (5–29 %) | I 1 tilstand |
| EDN3endothelin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| EDNRBendothelin receptor type B | Noen ganger (5–29 %) | I 1 tilstand |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Noen ganger (5–29 %) | I 1 tilstand |
| FCGR2AFc gamma receptor IIa | Noen ganger (5–29 %) | I 1 tilstand |
| FOXN1forkhead box N1 | Noen ganger (5–29 %) | I 1 tilstand |
| GALTgalactose-1-phosphate uridylyltransferase | Noen ganger (5–29 %) | I 2 tilstander |
| GDNFglial cell derived neurotrophic factor | Noen ganger (5–29 %) | I 1 tilstand |
| HBBhemoglobin subunit beta | Noen ganger (5–29 %) | I 2 tilstander |
| HEXBhexosaminidase subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| HMBShydroxymethylbilane synthase | Noen ganger (5–29 %) | I 2 tilstander |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Noen ganger (5–29 %) | I 2 tilstander |
| HTRA2HtrA serine peptidase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 1 | Noen ganger (5–29 %) | I 1 tilstand |
| IGKCimmunoglobulin kappa constant | Noen ganger (5–29 %) | I 1 tilstand |
| KARS1lysyl-tRNA synthetase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Noen ganger (5–29 %) | I 1 tilstand |
| LRRK2leucine rich repeat kinase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MLYCDmalonyl-CoA decarboxylase | Noen ganger (5–29 %) | I 2 tilstander |
| MMUTmethylmalonyl-CoA mutase | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Noen ganger (5–29 %) | I 1 tilstand |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Noen ganger (5–29 %) | I 1 tilstand |
| MYD88MYD88 innate immune signal transduction adaptor | Noen ganger (5–29 %) | I 1 tilstand |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Noen ganger (5–29 %) | I 1 tilstand |
| NAXDNAD(P)HX dehydratase | Noen ganger (5–29 %) | I 1 tilstand |
| NRTNneurturin | Noen ganger (5–29 %) | I 1 tilstand |
| PARK7Parkinsonism associated deglycase | Noen ganger (5–29 %) | I 1 tilstand |
| PINK1PTEN induced kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PMM2phosphomannomutase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| PODXLpodocalyxin like | Noen ganger (5–29 %) | I 1 tilstand |
| PRKNparkin RBR E3 ubiquitin protein ligase | Noen ganger (5–29 %) | I 1 tilstand |
| RETret proto-oncogene | Noen ganger (5–29 %) | I 2 tilstander |
| RNF168ring finger protein 168 | Noen ganger (5–29 %) | I 1 tilstand |
| SEMA3Csemaphorin 3C | Noen ganger (5–29 %) | I 1 tilstand |
| SEMA3Dsemaphorin 3D | Noen ganger (5–29 %) | I 1 tilstand |
| SLC22A5solute carrier family 22 member 5 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC37A4solute carrier family 37 member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SMOsmoothened, frizzled class receptor | Noen ganger (5–29 %) | I 1 tilstand |
| SMPD1sphingomyelin phosphodiesterase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SNCAsynuclein alpha | Noen ganger (5–29 %) | I 1 tilstand |
| SP110SP110 nuclear body protein | Noen ganger (5–29 %) | I 1 tilstand |
| SREBF1sterol regulatory element binding transcription factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Noen ganger (5–29 %) | I 1 tilstand |
| SYNJ1synaptojanin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TGFB1transforming growth factor beta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| TREHtrehalase | Noen ganger (5–29 %) | I 2 tilstander |
| UCHL1ubiquitin C-terminal hydrolase L1 | Noen ganger (5–29 %) | I 1 tilstand |
| VPS13Cvacuolar protein sorting 13 homolog C | Noen ganger (5–29 %) | I 1 tilstand |
| ZBTB24zinc finger and BTB domain containing 24 | Noen ganger (5–29 %) | I 1 tilstand |
| ZFYVE19zinc finger FYVE-type containing 19 | Noen ganger (5–29 %) | I 1 tilstand |
| C4Acomplement C4A (Chido/Rodgers blood group) | Sjelden (1–4%) | I 1 tilstand |
| CCR1C-C motif chemokine receptor 1 | Sjelden (1–4%) | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Sjelden (1–4%) | I 1 tilstand |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Sjelden (1–4%) | I 1 tilstand |
| FASFas cell surface death receptor | Sjelden (1–4%) | I 1 tilstand |
| IFNGR1interferon gamma receptor 1 | Sjelden (1–4%) | I 2 tilstander |
| IL10interleukin 10 | Sjelden (1–4%) | I 1 tilstand |
| IL12Ainterleukin 12A | Sjelden (1–4%) | I 1 tilstand |
| IL12A-AS1IL12A antisense RNA 1 | Sjelden (1–4%) | I 1 tilstand |
| IL23Rinterleukin 23 receptor | Sjelden (1–4%) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Sjelden (1–4%) | I 1 tilstand |
| KLRC4killer cell lectin like receptor C4 | Sjelden (1–4%) | I 1 tilstand |
| MAOAmonoamine oxidase A | Sjelden (1–4%) | I 1 tilstand |
| MGME1mitochondrial genome maintenance exonuclease 1 | Sjelden (1–4%) | I 1 tilstand |
| NAGSN-acetylglutamate synthase | Sjelden (1–4%) | I 1 tilstand |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Sjelden (1–4%) | I 1 tilstand |
| PHKBphosphorylase kinase regulatory subunit beta | Sjelden (1–4%) | I 2 tilstander |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Sjelden (1–4%) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Sjelden (1–4%) | I 1 tilstand |
| SLC12A3solute carrier family 12 member 3 | Sjelden (1–4%) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Sjelden (1–4%) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Sjelden (1–4%) | I 2 tilstander |
| TLR4toll like receptor 4 | Sjelden (1–4%) | I 1 tilstand |
| UBAC2UBA domain containing 2 | Sjelden (1–4%) | I 1 tilstand |
| ACSF3acyl-CoA synthetase family member 3 | Ikke registrert | I 1 tilstand |
| ACTG2actin gamma 2, smooth muscle | Ikke registrert | I 1 tilstand |
| AGAaspartylglucosaminidase | Ikke registrert | I 1 tilstand |
| AKR1D1aldo-keto reductase family 1 member D1 | Ikke registrert | I 1 tilstand |
| ALG3ALG3 alpha-1,3- mannosyltransferase | Ikke registrert | I 1 tilstand |
| ARXaristaless related homeobox | Ikke registrert | I 1 tilstand |
| BTDbiotinidase | Ikke registrert | I 1 tilstand |
| BTKBruton tyrosine kinase | Ikke registrert | I 1 tilstand |
| CD19CD19 molecule | Ikke registrert | I 1 tilstand |
| CFHcomplement factor H | Ikke registrert | I 1 tilstand |
| CFHR1complement factor H related 1 | Ikke registrert | I 1 tilstand |
| CFHR3complement factor H related 3 | Ikke registrert | I 1 tilstand |
| CPOXcoproporphyrinogen oxidase | Ikke registrert | I 1 tilstand |
| CR2complement C3d receptor 2 | Ikke registrert | I 1 tilstand |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Ikke registrert | I 1 tilstand |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Ikke registrert | I 1 tilstand |
| DCLRE1CDNA cross-link repair 1C | Ikke registrert | I 1 tilstand |
| DESdesmin | Ikke registrert | I 1 tilstand |
| DNMT3BDNA methyltransferase 3 beta | Ikke registrert | I 1 tilstand |
| ELP1elongator acetyltransferase complex subunit 1 | Ikke registrert | I 1 tilstand |
| GLAgalactosidase alpha | Ikke registrert | I 1 tilstand |
| GNSglucosamine (N-acetyl)-6-sulfatase | Ikke registrert | I 1 tilstand |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Ikke registrert | I 1 tilstand |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Ikke registrert | I 1 tilstand |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Ikke registrert | I 1 tilstand |
| HS3ST6heparan sulfate-glucosamine 3-sulfotransferase 6 | Ikke registrert | I 1 tilstand |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Ikke registrert | I 1 tilstand |
| ICOSinducible T cell costimulator | Ikke registrert | I 2 tilstander |
| IDSiduronate 2-sulfatase | Ikke registrert | I 1 tilstand |
| IFNGinterferon gamma | Ikke registrert | I 1 tilstand |
| IL6interleukin 6 | Ikke registrert | I 1 tilstand |
| IL7Rinterleukin 7 receptor | Ikke registrert | I 1 tilstand |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Ikke registrert | I 1 tilstand |
| KIF1Bkinesin family member 1B | Ikke registrert | I 1 tilstand |
| LCTlactase | Ikke registrert | I 1 tilstand |
| MCM6minichromosome maintenance complex component 6 | Ikke registrert | I 1 tilstand |
| NAGLUN-acetyl-alpha-glucosaminidase | Ikke registrert | I 1 tilstand |
| NBNnibrin | Ikke registrert | I 1 tilstand |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Ikke registrert | I 1 tilstand |
| OPLAH5-oxoprolinase, ATP-hydrolysing | Ikke registrert | I 1 tilstand |
| PCSK1proprotein convertase subtilisin/kexin type 1 | Ikke registrert | I 1 tilstand |
| PSTPIP1proline-serine-threonine phosphatase interacting protein 1 | Ikke registrert | I 1 tilstand |
| RAG1recombination activating 1 | Ikke registrert | I 2 tilstander |
| RAG2recombination activating 2 | Ikke registrert | I 2 tilstander |
| RFX6regulatory factor X6 | Ikke registrert | I 1 tilstand |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Ikke registrert | I 1 tilstand |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Ikke registrert | I 1 tilstand |
| SCNN1Asodium channel epithelial 1 subunit alpha | Ikke registrert | I 1 tilstand |
| SLC12A1solute carrier family 12 member 1 | Ikke registrert | I 1 tilstand |
| SUGCTsuccinyl-CoA:glutarate-CoA transferase | Ikke registrert | I 1 tilstand |
| TLK2tousled like kinase 2 | Ikke registrert | I 1 tilstand |
| TMPRSS15transmembrane serine protease 15 | Ikke registrert | I 1 tilstand |
| TNFRSF13BTNF receptor superfamily member 13B | Ikke registrert | I 1 tilstand |
| TNFRSF13CTNF receptor superfamily member 13C | Ikke registrert | I 1 tilstand |
| WASWASP actin nucleation promoting factor | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.18-8b139e39.
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