Tunnus
Fluid retention
Kliiniline nimetus: Edema
An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body.
Kokkuvõte
- Teised nimetused
- Water retention, Dropsy, Hydrops, Oedema
- Kehasüsteem
- Laboratory abnormality
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Fluid retention, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test227 geeni on seotud tunnusega Fluid retention
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Fluid retention. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| ALBalbumin | Alati | Esineb 2 haiguses |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Alati | Esineb 2 haiguses |
| ATP7BATPase copper transporting beta | Alati | Esineb 1 haiguses |
| CCDC88Acoiled-coil and HOOK domain protein 88A | Alati | Esineb 1 haiguses |
| DCLRE1CDNA cross-link repair 1C | Alati | Esineb 2 haiguses |
| IFT140intraflagellar transport 140 | Alati | Esineb 1 haiguses |
| MRPS16mitochondrial ribosomal protein S16 | Alati | Esineb 1 haiguses |
| MYO1Emyosin IE | Alati | Esineb 2 haiguses |
| OTULINOTU deubiquitinase with linear linkage specificity | Alati | Esineb 1 haiguses |
| PDSS2decaprenyl diphosphate synthase subunit 2 | Alati | Esineb 1 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alati | Esineb 1 haiguses |
| PSMG2proteasome assembly chaperone 2 | Alati | Esineb 1 haiguses |
| PTPROprotein tyrosine phosphatase receptor type O | Alati | Esineb 2 haiguses |
| RAG1recombination activating 1 | Alati | Esineb 2 haiguses |
| RAG2recombination activating 2 | Alati | Esineb 2 haiguses |
| SCARB2scavenger receptor class B member 2 | Alati | Esineb 1 haiguses |
| SPOUT1SPOUT domain containing methyltransferase 1 | Alati | Esineb 1 haiguses |
| VPS51VPS51 subunit of GARP complex | Alati | Esineb 1 haiguses |
| ACTN4actinin alpha 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| AGBL1AGBL carboxypeptidase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANKFY1ankyrin repeat and FYVE domain containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANLNanillin, actin binding protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| APOL1apolipoprotein L1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ARHGAP24Rho GTPase activating protein 24 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ARHGDIARho GDP dissociation inhibitor alpha | Väga sageli (80–99%) | Esineb 2 haiguses |
| AVILadvillin | Väga sageli (80–99%) | Esineb 1 haiguses |
| CD2APCD2 associated protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CD55CD55 molecule (Cromer blood group) | Väga sageli (80–99%) | Esineb 1 haiguses |
| COL4A3collagen type IV alpha 3 chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| COL8A2collagen type VIII alpha 2 chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| COQ8Bcoenzyme Q8B | Väga sageli (80–99%) | Esineb 2 haiguses |
| CRB2crumbs cell polarity complex component 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DAAM2dishevelled associated activator of morphogenesis 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| EMP2epithelial membrane protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GAPVD1GTPase activating protein and VPS9 domains 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| INF2inverted formin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KANK2KN motif and ankyrin repeat domains 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRT2keratin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LAMA5laminin subunit alpha 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAGI2membrane associated guanylate kinase, WW and PDZ domain containing 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
Näita veel 187 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| MAPRE2microtubule associated protein RP/EB family member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NPHS1NPHS1 adhesion molecule, nephrin | Väga sageli (80–99%) | Esineb 2 haiguses |
| NPHS2NPHS2 stomatin family member, podocin | Väga sageli (80–99%) | Esineb 2 haiguses |
| NUP107nucleoporin 107 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NUP133nucleoporin 133 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP160nucleoporin 160 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP205nucleoporin 205 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP37nucleoporin 37 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP85nucleoporin 85 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP93nucleoporin 93 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PAX2paired box 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| PLCE1phospholipase C epsilon 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC4A11solute carrier family 4 member 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TBC1D8BTBC1 domain family member 8B | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TRPC6transient receptor potential cation channel subfamily C member 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TUBBtubulin beta class I | Väga sageli (80–99%) | Esineb 1 haiguses |
| WT1WT1 transcription factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZEB1zinc finger E-box binding homeobox 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ABCC9ATP binding cassette subfamily C member 9 | Sageli (30–79%) | Esineb 1 haiguses |
| ACTC1actin alpha cardiac muscle 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ACTN2actinin alpha 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ADAadenosine deaminase | Sageli (30–79%) | Esineb 1 haiguses |
| ANKRD1ankyrin repeat domain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BAG3BAG cochaperone 3 | Sageli (30–79%) | Esineb 1 haiguses |
| BAG5BAG cochaperone 5 | Sageli (30–79%) | Esineb 1 haiguses |
| CAP2cyclase associated actin cytoskeleton regulatory protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| CHD7chromodomain helicase DNA binding protein 7 | Sageli (30–79%) | Esineb 1 haiguses |
| COL2A1collagen type II alpha 1 chain | Sageli (30–79%) | Esineb 2 haiguses |
| CRYABcrystallin alpha B | Sageli (30–79%) | Esineb 1 haiguses |
| CSRP3cysteine and glycine rich protein 3 | Sageli (30–79%) | Esineb 1 haiguses |
| DESdesmin | Sageli (30–79%) | Esineb 1 haiguses |
| DGKEdiacylglycerol kinase epsilon | Sageli (30–79%) | Esineb 1 haiguses |
| DMDdystrophin | Sageli (30–79%) | Esineb 1 haiguses |
| DOLKdolichol kinase | Sageli (30–79%) | Esineb 1 haiguses |
| DSG2desmoglein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| DSPdesmoplakin | Sageli (30–79%) | Esineb 2 haiguses |
| FHL2four and a half LIM domains 2 | Sageli (30–79%) | Esineb 1 haiguses |
| FKTNfukutin | Sageli (30–79%) | Esineb 1 haiguses |
| FLNCfilamin C | Sageli (30–79%) | Esineb 1 haiguses |
| GATAD1GATA zinc finger domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Sageli (30–79%) | Esineb 1 haiguses |
| GNA14G protein subunit alpha 14 | Sageli (30–79%) | Esineb 1 haiguses |
| GSNgelsolin | Sageli (30–79%) | Esineb 1 haiguses |
| HAND2heart and neural crest derivatives expressed 2 | Sageli (30–79%) | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| HPGD15-hydroxyprostaglandin dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| IFIH1interferon induced with helicase C domain 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IL2RGinterleukin 2 receptor subunit gamma | Sageli (30–79%) | Esineb 1 haiguses |
| IL7Rinterleukin 7 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| IRAK1interleukin 1 receptor associated kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| JPH2junctophilin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KIF11kinesin family member 11 | Sageli (30–79%) | Esineb 1 haiguses |
| LAMA4laminin subunit alpha 4 | Sageli (30–79%) | Esineb 1 haiguses |
| LDB3LIM domain binding 3 | Sageli (30–79%) | Esineb 1 haiguses |
| LMNAlamin A/C | Sageli (30–79%) | Esineb 1 haiguses |
| LMOD2leiomodin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| LPIN2lipin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MAGEL2MAGE family member L2 | Sageli (30–79%) | Esineb 1 haiguses |
| MKRN3makorin ring finger protein 3 | Sageli (30–79%) | Esineb 1 haiguses |
| MPImannose phosphate isomerase | Sageli (30–79%) | Esineb 2 haiguses |
| MVKmevalonate kinase | Sageli (30–79%) | Esineb 1 haiguses |
| MYBPC3myosin binding protein C3 | Sageli (30–79%) | Esineb 1 haiguses |
| MYH6myosin heavy chain 6 | Sageli (30–79%) | Esineb 1 haiguses |
| MYH7myosin heavy chain 7 | Sageli (30–79%) | Esineb 1 haiguses |
| MYPNmyopalladin | Sageli (30–79%) | Esineb 1 haiguses |
| NEU1neuraminidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NEXNnexilin F-actin binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Sageli (30–79%) | Esineb 1 haiguses |
| NPAP1nuclear pore associated protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NRAPnebulin related anchoring protein | Sageli (30–79%) | Esineb 1 haiguses |
| NUDCD3NudC domain containing 3 | Sageli (30–79%) | Esineb 1 haiguses |
| PLNphospholamban | Sageli (30–79%) | Esineb 1 haiguses |
| PPCSphosphopantothenoylcysteine synthetase | Sageli (30–79%) | Esineb 1 haiguses |
| PRDM16PR/SET domain 16 | Sageli (30–79%) | Esineb 1 haiguses |
| PRF1perforin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PSAT1phosphoserine aminotransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PSEN2presenilin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| PSMB10proteasome 20S subunit beta 10 | Sageli (30–79%) | Esineb 1 haiguses |
| PWAR1Prader Willi/Angelman region RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Sageli (30–79%) | Esineb 1 haiguses |
| RBM20RNA binding motif protein 20 | Sageli (30–79%) | Esineb 1 haiguses |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sageli (30–79%) | Esineb 1 haiguses |
| RPL3Lribosomal protein L3 like | Sageli (30–79%) | Esineb 1 haiguses |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Sageli (30–79%) | Esineb 1 haiguses |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| SGCDsarcoglycan delta | Sageli (30–79%) | Esineb 1 haiguses |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Sageli (30–79%) | Esineb 1 haiguses |
| SPP1secreted phosphoprotein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| STAT4signal transducer and activator of transcription 4 | Sageli (30–79%) | Esineb 1 haiguses |
| STX11syntaxin 11 | Sageli (30–79%) | Esineb 1 haiguses |
| TAF1ATATA-box binding protein associated factor, RNA polymerase I subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Sageli (30–79%) | Esineb 1 haiguses |
| TALDO1transaldolase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TCAPtitin-cap | Sageli (30–79%) | Esineb 1 haiguses |
| TMPOthymopoietin | Sageli (30–79%) | Esineb 1 haiguses |
| TNNC1troponin C1, slow skeletal and cardiac type | Sageli (30–79%) | Esineb 1 haiguses |
| TNNI3troponin I3, cardiac type | Sageli (30–79%) | Esineb 1 haiguses |
| TNNT2troponin T2, cardiac type | Sageli (30–79%) | Esineb 1 haiguses |
| TPM1tropomyosin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TPRKBTP53RK binding protein | Sageli (30–79%) | Esineb 1 haiguses |
| TTNtitin | Sageli (30–79%) | Esineb 1 haiguses |
| TXNRD2thioredoxin reductase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| VCLvinculin | Sageli (30–79%) | Esineb 1 haiguses |
| VEZF1vascular endothelial zinc finger 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCC6ATP binding cassette subfamily C member 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACAT1acetyl-CoA acetyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| AGGF1angiogenic factor with G-patch and FHA domains 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| B4GALT1beta-1,4-galactosyltransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD28CD28 molecule | Mõnikord (5–29%) | Esineb 2 haiguses |
| CFTRCF transmembrane conductance regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ENGendoglin | Mõnikord (5–29%) | Esineb 1 haiguses |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FECHferrochelatase | Mõnikord (5–29%) | Esineb 2 haiguses |
| GNAQG protein subunit alpha q | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Mõnikord (5–29%) | Esineb 1 haiguses |
| JAG1jagged canonical Notch ligand 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMA3laminin subunit alpha 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMB3laminin subunit beta 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMC2laminin subunit gamma 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LYSTlysosomal trafficking regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| MOGSmannosyl-oligosaccharide glucosidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PBX1PBX homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Mõnikord (5–29%) | Esineb 2 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PMM2phosphomannomutase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RNU7-1RNA, U7 small nuclear 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TNFRSF1BTNF receptor superfamily member 1B | Mõnikord (5–29%) | Esineb 2 haiguses |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZNFX1zinc finger NFX1-type containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACBD6acyl-CoA binding domain containing 6 | Harva (1–4%) | Esineb 1 haiguses |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Harva (1–4%) | Esineb 2 haiguses |
| DUOX2dual oxidase 2 | Harva (1–4%) | Esineb 1 haiguses |
| GATA1GATA binding protein 1 | Harva (1–4%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Harva (1–4%) | Esineb 1 haiguses |
| POLG2DNA polymerase gamma 2, accessory subunit | Harva (1–4%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Harva (1–4%) | Esineb 1 haiguses |
| SLC25A4solute carrier family 25 member 4 | Harva (1–4%) | Esineb 1 haiguses |
| TSHRthyroid stimulating hormone receptor | Harva (1–4%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Harva (1–4%) | Esineb 1 haiguses |
| URODuroporphyrinogen decarboxylase | Harva (1–4%) | Esineb 1 haiguses |
| UROSuroporphyrinogen III synthase | Harva (1–4%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Pole registreeritud | Esineb 1 haiguses |
| BLTP1bridge-like lipid transfer protein family member 1 | Pole registreeritud | Esineb 1 haiguses |
| BPTFbromodomain PHD finger transcription factor | Pole registreeritud | Esineb 1 haiguses |
| BSNDbarttin CLCNK type accessory subunit beta | Pole registreeritud | Esineb 1 haiguses |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Pole registreeritud | Esineb 1 haiguses |
| CHRNDcholinergic receptor nicotinic delta subunit | Pole registreeritud | Esineb 1 haiguses |
| CHRNGcholinergic receptor nicotinic gamma subunit | Pole registreeritud | Esineb 1 haiguses |
| CLCNKAchloride voltage-gated channel Ka | Pole registreeritud | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Pole registreeritud | Esineb 1 haiguses |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Pole registreeritud | Esineb 1 haiguses |
| EBPEBP cholestenol delta-isomerase | Pole registreeritud | Esineb 1 haiguses |
| EPHB4EPH receptor B4 | Pole registreeritud | Esineb 1 haiguses |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Pole registreeritud | Esineb 1 haiguses |
| ERCC5ERCC excision repair 5, endonuclease | Pole registreeritud | Esineb 1 haiguses |
| FGAfibrinogen alpha chain | Pole registreeritud | Esineb 1 haiguses |
| GBE11,4-alpha-glucan branching enzyme 1 | Pole registreeritud | Esineb 1 haiguses |
| GLE1GLE1 RNA export mediator | Pole registreeritud | Esineb 1 haiguses |
| IL6interleukin 6 | Pole registreeritud | Esineb 1 haiguses |
| INPPL1inositol polyphosphate phosphatase like 1 | Pole registreeritud | Esineb 1 haiguses |
| KITKIT proto-oncogene, receptor tyrosine kinase | Pole registreeritud | Esineb 1 haiguses |
| KRT13keratin 13 | Pole registreeritud | Esineb 1 haiguses |
| LAMB2laminin subunit beta 2 | Pole registreeritud | Esineb 1 haiguses |
| MKKSMKKS centrosomal shuttling protein | Pole registreeritud | Esineb 1 haiguses |
| MRPS22mitochondrial ribosomal protein S22 | Pole registreeritud | Esineb 1 haiguses |
| NR2E3nuclear receptor subfamily 2 group E member 3 | Pole registreeritud | Esineb 1 haiguses |
| NRASNRAS proto-oncogene, GTPase | Pole registreeritud | Esineb 1 haiguses |
| OSGEPO-sialoglycoprotein endopeptidase | Pole registreeritud | Esineb 1 haiguses |
| PLD1phospholipase D1 | Pole registreeritud | Esineb 1 haiguses |
| SGPL1sphingosine-1-phosphate lyase 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC26A2solute carrier family 26 member 2 | Pole registreeritud | Esineb 1 haiguses |
| TREX1three prime repair exonuclease 1 | Pole registreeritud | Esineb 1 haiguses |
| USP8ubiquitin specific peptidase 8 | Pole registreeritud | Esineb 1 haiguses |
| ZNHIT3zinc finger HIT-type containing 3 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
- Fluid around lungs86 geeni
- Swelling caused by excess lymph fluid under skin75 geeni
- Hydrops fetalis71 geeni
- Increased nuchal translucency66 geeni
- Fluid accumulation in lower limbs53 geeni
- Joint swelling53 geeni
- Facial puffiness35 geeni
- Brain swelling32 geeni
- Excess fluid in lungs30 geeni
- Generalized edema18 geeni
- Edema of the dorsum of hands16 geeni
- Angioedema13 geeni
- Corneal stromal edema13 geeni
- Peripheral edema11 geeni
- Laryngeal edema5 geeni
- Fetal skin edema4 geeni
- Genital edema4 geeni
- Peau d'orange4 geeni
- Throat swelling3 geeni
- Intestinal edema2 geeni
- Tongue edema2 geeni
- Hyperkeratosis over edematous areas1 geen
- Hypoproteinemic edema1 geen
- Muscular edema1 geen
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast