Egenskap
Chronic diarrhea
The presence of chronic diarrhea, which is usually taken to mean diarrhea that has persisted for over 4 weeks.
Sammendrag
- Også kalt
- Diarrhea, recurrent, Recurrent diarrhea, Chronic diarrhoea
- Kroppssystem
- Abnormality of the digestive system
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Få mitt Genome Test124 gener knyttet til Chronic diarrhea
Endringer i disse genene forårsaker sjeldne tilstander der Chronic 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 |
|---|---|---|
| ADAadenosine deaminase | Alltid | I 2 tilstander |
| ATP6AP1ATPase H+ transporting accessory protein 1 | Alltid | I 1 tilstand |
| B2Mbeta-2-microglobulin | Alltid | I 1 tilstand |
| BACH2BACH transcriptional regulator 2 | Alltid | I 1 tilstand |
| CARD8caspase recruitment domain family member 8 | Alltid | I 1 tilstand |
| CD3GCD3 gamma subunit of T-cell receptor complex | Alltid | I 1 tilstand |
| CHASERRCHD2 adjacent suppressive regulatory RNA | Alltid | I 1 tilstand |
| CLMPCXADR like cell adhesion molecule | Alltid | I 1 tilstand |
| CR2complement C3d receptor 2 | Alltid | I 1 tilstand |
| DCLRE1CDNA cross-link repair 1C | Alltid | I 2 tilstander |
| DNASE2deoxyribonuclease 2, lysosomal | Alltid | I 1 tilstand |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Alltid | I 1 tilstand |
| FOXP3forkhead box P3 | Alltid | I 1 tilstand |
| GUCY2Cguanylate cyclase 2C | Alltid | I 2 tilstander |
| HYOU1hypoxia up-regulated 1 | Alltid | I 1 tilstand |
| IGKCimmunoglobulin kappa constant | Alltid | I 1 tilstand |
| IKZF2IKAROS family zinc finger 2 | Alltid | I 1 tilstand |
| IL2RAinterleukin 2 receptor subunit alpha | Alltid | I 1 tilstand |
| IL6STinterleukin 6 cytokine family signal transducer | Alltid | I 1 tilstand |
| ITGB2integrin subunit beta 2 | Alltid | I 1 tilstand |
| JAK3Janus kinase 3 | Alltid | I 2 tilstander |
| MAN2B2mannosidase alpha class 2B member 2 | Alltid | I 1 tilstand |
| NDC1NDC1 transmembrane nucleoporin | Alltid | I 1 tilstand |
| NFKBIANFKB inhibitor alpha | Alltid | I 2 tilstander |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Alltid | I 1 tilstand |
| PTCRApre T cell antigen receptor alpha | Alltid | I 1 tilstand |
| RELREL proto-oncogene, NF-kB subunit | Alltid | I 1 tilstand |
| SAMD9sterile alpha motif domain containing 9 | Alltid | I 1 tilstand |
| SKIC2SKI2 subunit of superkiller complex | Alltid | I 1 tilstand |
| SLC10A2solute carrier family 10 member 2 | Alltid | I 1 tilstand |
| SLC19A1solute carrier family 19 member 1 | Alltid | I 1 tilstand |
| SLC51Asolute carrier family 51 member A | Alltid | I 1 tilstand |
| SLC51BSLC51 subunit beta | Alltid | I 1 tilstand |
| SLC5A1solute carrier family 5 member 1 | Alltid | I 1 tilstand |
| STX3syntaxin 3 | Alltid | I 1 tilstand |
| TCF3transcription factor 3 | Alltid | I 1 tilstand |
| TOM1target of myb1 membrane trafficking protein | Alltid | I 1 tilstand |
| TRAF3TNF receptor associated factor 3 | Alltid | I 1 tilstand |
| VPS45vacuolar protein sorting 45 homolog | Alltid | I 1 tilstand |
| ZAP70zeta chain of T cell receptor associated protein kinase 70 | Alltid | I 2 tilstander |
Vis 84 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ANTXR2ANTXR cell adhesion molecule 2 | Svært ofte (80–99 %) | I 1 tilstand |
| BTKBruton tyrosine kinase | Svært ofte (80–99 %) | I 2 tilstander |
| CHD7chromodomain helicase DNA binding protein 7 | Svært ofte (80–99 %) | I 1 tilstand |
| EPCAMepithelial cell adhesion molecule | Svært ofte (80–99 %) | I 1 tilstand |
| IL2RGinterleukin 2 receptor subunit gamma | Svært ofte (80–99 %) | I 2 tilstander |
| IL7Rinterleukin 7 receptor | Svært ofte (80–99 %) | I 2 tilstander |
| NBNnibrin | Svært ofte (80–99 %) | I 1 tilstand |
| NUDCD3NudC domain containing 3 | Svært ofte (80–99 %) | I 1 tilstand |
| PSMB10proteasome 20S subunit beta 10 | Svært ofte (80–99 %) | I 1 tilstand |
| RAG1recombination activating 1 | Svært ofte (80–99 %) | I 1 tilstand |
| RAG2recombination activating 2 | Svært ofte (80–99 %) | I 1 tilstand |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Svært ofte (80–99 %) | I 1 tilstand |
| SLC39A4solute carrier family 39 member 4 | Svært ofte (80–99 %) | I 1 tilstand |
| WASWASP actin nucleation promoting factor | Svært ofte (80–99 %) | I 2 tilstander |
| AGR2anterior gradient 2, protein disulphide isomerase family member | Ofte (30–79 %) | I 1 tilstand |
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Ofte (30–79 %) | I 1 tilstand |
| ALKALK receptor tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| ATMATM serine/threonine kinase | Ofte (30–79 %) | I 1 tilstand |
| ATP5F1AATP synthase F1 subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| ATP7AATPase copper transporting alpha | Ofte (30–79 %) | I 1 tilstand |
| CASP8caspase 8 | Ofte (30–79 %) | I 1 tilstand |
| CD3DCD3 delta subunit of T-cell receptor complex | Ofte (30–79 %) | I 1 tilstand |
| COG6component of oligomeric golgi complex 6 | Ofte (30–79 %) | I 1 tilstand |
| CYP27A1cytochrome P450 family 27 subfamily A member 1 | Ofte (30–79 %) | I 1 tilstand |
| ETHE1ETHE1 persulfide dioxygenase | Ofte (30–79 %) | I 1 tilstand |
| FCHO1FCH and mu domain containing endocytic adaptor 1 | Ofte (30–79 %) | I 1 tilstand |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Ofte (30–79 %) | I 1 tilstand |
| IDUAalpha-L-iduronidase | Ofte (30–79 %) | I 1 tilstand |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Ofte (30–79 %) | I 1 tilstand |
| IL21Rinterleukin 21 receptor | Ofte (30–79 %) | I 1 tilstand |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Ofte (30–79 %) | I 1 tilstand |
| IRF4interferon regulatory factor 4 | Ofte (30–79 %) | I 1 tilstand |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Ofte (30–79 %) | I 1 tilstand |
| LMO1LIM domain only 1 | Ofte (30–79 %) | I 1 tilstand |
| LRBALPS responsive beige-like anchor protein | Ofte (30–79 %) | I 1 tilstand |
| MADDMAP kinase activating death domain | Ofte (30–79 %) | I 2 tilstander |
| MAP3K14mitogen-activated protein kinase kinase kinase 14 | Ofte (30–79 %) | I 1 tilstand |
| MGME1mitochondrial genome maintenance exonuclease 1 | Ofte (30–79 %) | I 1 tilstand |
| MTTPmicrosomal triglyceride transfer protein | Ofte (30–79 %) | I 1 tilstand |
| MVKmevalonate kinase | Ofte (30–79 %) | I 1 tilstand |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Ofte (30–79 %) | I 1 tilstand |
| ORAI1ORAI calcium release-activated calcium modulator 1 | Ofte (30–79 %) | I 1 tilstand |
| OTULINOTU deubiquitinase with linear linkage specificity | Ofte (30–79 %) | I 1 tilstand |
| PHOX2Bpaired like homeobox 2B | Ofte (30–79 %) | I 1 tilstand |
| POLA1DNA polymerase alpha 1, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| RBCK1RANBP2-type and C3HC4-type zinc finger containing 1 | Ofte (30–79 %) | I 1 tilstand |
| RFXANKregulatory factor X associated ankyrin containing protein | Ofte (30–79 %) | I 1 tilstand |
| RYR3ryanodine receptor 3 | Ofte (30–79 %) | I 1 tilstand |
| SAA1serum amyloid A1 | Ofte (30–79 %) | I 1 tilstand |
| SPINK5serine peptidase inhibitor Kazal type 5 | Ofte (30–79 %) | I 2 tilstander |
| TFRCtransferrin receptor | Ofte (30–79 %) | I 1 tilstand |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Ofte (30–79 %) | I 1 tilstand |
| VPS33BVPS33B late endosome and lysosome associated | Ofte (30–79 %) | I 1 tilstand |
| ADNPactivity dependent neuroprotector homeobox | Noen ganger (5–29 %) | I 1 tilstand |
| CARD11caspase recruitment domain family member 11 | Noen ganger (5–29 %) | I 1 tilstand |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CCDC47coiled-coil domain containing 47 | Noen ganger (5–29 %) | I 1 tilstand |
| COG4component of oligomeric golgi complex 4 | Noen ganger (5–29 %) | I 1 tilstand |
| DOCK2dedicator of cytokinesis 2 | Noen ganger (5–29 %) | I 1 tilstand |
| GINS3GINS complex subunit 3 | Noen ganger (5–29 %) | I 1 tilstand |
| HEATR3HEAT repeat containing 3 | Noen ganger (5–29 %) | I 1 tilstand |
| IGHMimmunoglobulin heavy constant mu | Noen ganger (5–29 %) | I 1 tilstand |
| IPO8importin 8 | Noen ganger (5–29 %) | I 1 tilstand |
| ITCHitchy E3 ubiquitin protein ligase | Noen ganger (5–29 %) | I 1 tilstand |
| KMT5Blysine methyltransferase 5B | Noen ganger (5–29 %) | I 1 tilstand |
| PGM1phosphoglucomutase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PKP1plakophilin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Noen ganger (5–29 %) | I 2 tilstander |
| SLC35C1solute carrier family 35 member C1 | Noen ganger (5–29 %) | I 1 tilstand |
| SONSON DNA and RNA binding protein | Noen ganger (5–29 %) | I 2 tilstander |
| SREBF1sterol regulatory element binding transcription factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| STAT5Bsignal transducer and activator of transcription 5B | Noen ganger (5–29 %) | I 1 tilstand |
| TNFRSF1ATNF receptor superfamily member 1A | Noen ganger (5–29 %) | I 1 tilstand |
| USP7ubiquitin specific peptidase 7 | Noen ganger (5–29 %) | I 1 tilstand |
| WDR83OSWD repeat domain 83 opposite strand | Noen ganger (5–29 %) | I 1 tilstand |
| ASAH1N-acylsphingosine amidohydrolase 1 | Sjelden (1–4%) | I 1 tilstand |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sjelden (1–4%) | I 1 tilstand |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Ikke registrert | I 1 tilstand |
| FOXN1forkhead box N1 | Ikke registrert | I 1 tilstand |
| HEXBhexosaminidase subunit beta | Ikke registrert | I 1 tilstand |
| IKBKBinhibitor of nuclear factor kappa B kinase subunit beta | Ikke registrert | I 1 tilstand |
| RNF113Aring finger protein 113A | Ikke registrert | I 1 tilstand |
| TERTtelomerase reverse transcriptase | Ikke registrert | I 1 tilstand |
| TKFCtriokinase and FMN cyclase | 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.
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 2026.10.16-c6eea6bf.
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