Egenskap
Fluid retention
Klinisk navn: Edema
An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body.
Sammendrag
- Også kalt
- Water retention, Dropsy, Hydrops, Oedema
- Kroppssystem
- Laboratory abnormality
ReferansegenomGRCh38hg38
Posisjoner på gen- og variantsidene følger dette valget i denne nettleseren.
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Få mitt Genome Test227 gener knyttet til Fluid retention
Endringer i disse genene forårsaker sjeldne tilstander der Fluid retention 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 |
|---|---|---|
| ALBalbumin | Alltid | I 2 tilstander |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Alltid | I 2 tilstander |
| ATP7BATPase copper transporting beta | Alltid | I 1 tilstand |
| CCDC88Acoiled-coil and HOOK domain protein 88A | Alltid | I 1 tilstand |
| DCLRE1CDNA cross-link repair 1C | Alltid | I 2 tilstander |
| IFT140intraflagellar transport 140 | Alltid | I 1 tilstand |
| MRPS16mitochondrial ribosomal protein S16 | Alltid | I 1 tilstand |
| MYO1Emyosin IE | Alltid | I 2 tilstander |
| OTULINOTU deubiquitinase with linear linkage specificity | Alltid | I 1 tilstand |
| PDSS2decaprenyl diphosphate synthase subunit 2 | Alltid | I 1 tilstand |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alltid | I 1 tilstand |
| PSMG2proteasome assembly chaperone 2 | Alltid | I 1 tilstand |
| PTPROprotein tyrosine phosphatase receptor type O | Alltid | I 2 tilstander |
| RAG1recombination activating 1 | Alltid | I 2 tilstander |
| RAG2recombination activating 2 | Alltid | I 2 tilstander |
| SCARB2scavenger receptor class B member 2 | Alltid | I 1 tilstand |
| SPOUT1SPOUT domain containing methyltransferase 1 | Alltid | I 1 tilstand |
| VPS51VPS51 subunit of GARP complex | Alltid | I 1 tilstand |
| ACTN4actinin alpha 4 | Svært ofte (80–99 %) | I 2 tilstander |
| AGBL1AGBL carboxypeptidase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| ANKFY1ankyrin repeat and FYVE domain containing 1 | Svært ofte (80–99 %) | I 1 tilstand |
| ANLNanillin, actin binding protein | Svært ofte (80–99 %) | I 1 tilstand |
| APOL1apolipoprotein L1 | Svært ofte (80–99 %) | I 1 tilstand |
| ARHGAP24Rho GTPase activating protein 24 | Svært ofte (80–99 %) | I 1 tilstand |
| ARHGDIARho GDP dissociation inhibitor alpha | Svært ofte (80–99 %) | I 2 tilstander |
| AVILadvillin | Svært ofte (80–99 %) | I 1 tilstand |
| CD2APCD2 associated protein | Svært ofte (80–99 %) | I 1 tilstand |
| CD55CD55 molecule (Cromer blood group) | Svært ofte (80–99 %) | I 1 tilstand |
| COL4A3collagen type IV alpha 3 chain | Svært ofte (80–99 %) | I 1 tilstand |
| COL8A2collagen type VIII alpha 2 chain | Svært ofte (80–99 %) | I 1 tilstand |
| COQ8Bcoenzyme Q8B | Svært ofte (80–99 %) | I 2 tilstander |
| CRB2crumbs cell polarity complex component 2 | Svært ofte (80–99 %) | I 1 tilstand |
| DAAM2dishevelled associated activator of morphogenesis 2 | Svært ofte (80–99 %) | I 1 tilstand |
| EMP2epithelial membrane protein 2 | Svært ofte (80–99 %) | I 1 tilstand |
| GAPVD1GTPase activating protein and VPS9 domains 1 | Svært ofte (80–99 %) | I 1 tilstand |
| INF2inverted formin 2 | Svært ofte (80–99 %) | I 1 tilstand |
| KANK2KN motif and ankyrin repeat domains 2 | Svært ofte (80–99 %) | I 1 tilstand |
| KRT2keratin 2 | Svært ofte (80–99 %) | I 1 tilstand |
| LAMA5laminin subunit alpha 5 | Svært ofte (80–99 %) | I 1 tilstand |
| MAGI2membrane associated guanylate kinase, WW and PDZ domain containing 2 | Svært ofte (80–99 %) | I 1 tilstand |
Vis 187 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| MAPRE2microtubule associated protein RP/EB family member 2 | Svært ofte (80–99 %) | I 1 tilstand |
| NPHS1NPHS1 adhesion molecule, nephrin | Svært ofte (80–99 %) | I 2 tilstander |
| NPHS2NPHS2 stomatin family member, podocin | Svært ofte (80–99 %) | I 2 tilstander |
| NUP107nucleoporin 107 | Svært ofte (80–99 %) | I 2 tilstander |
| NUP133nucleoporin 133 | Svært ofte (80–99 %) | I 1 tilstand |
| NUP160nucleoporin 160 | Svært ofte (80–99 %) | I 1 tilstand |
| NUP205nucleoporin 205 | Svært ofte (80–99 %) | I 1 tilstand |
| NUP37nucleoporin 37 | Svært ofte (80–99 %) | I 1 tilstand |
| NUP85nucleoporin 85 | Svært ofte (80–99 %) | I 1 tilstand |
| NUP93nucleoporin 93 | Svært ofte (80–99 %) | I 1 tilstand |
| PAX2paired box 2 | Svært ofte (80–99 %) | I 3 tilstander |
| PLCE1phospholipase C epsilon 1 | Svært ofte (80–99 %) | I 2 tilstander |
| SLC4A11solute carrier family 4 member 11 | Svært ofte (80–99 %) | I 1 tilstand |
| TBC1D8BTBC1 domain family member 8B | Svært ofte (80–99 %) | I 1 tilstand |
| TCF4transcription factor 4 | Svært ofte (80–99 %) | I 1 tilstand |
| TRPC6transient receptor potential cation channel subfamily C member 6 | Svært ofte (80–99 %) | I 1 tilstand |
| TUBBtubulin beta class I | Svært ofte (80–99 %) | I 1 tilstand |
| WT1WT1 transcription factor | Svært ofte (80–99 %) | I 1 tilstand |
| ZEB1zinc finger E-box binding homeobox 1 | Svært ofte (80–99 %) | I 1 tilstand |
| ABCC9ATP binding cassette subfamily C member 9 | Ofte (30–79 %) | I 1 tilstand |
| ACTC1actin alpha cardiac muscle 1 | Ofte (30–79 %) | I 1 tilstand |
| ACTN2actinin alpha 2 | Ofte (30–79 %) | I 1 tilstand |
| ADAadenosine deaminase | Ofte (30–79 %) | I 1 tilstand |
| ANKRD1ankyrin repeat domain 1 | Ofte (30–79 %) | I 1 tilstand |
| BAG3BAG cochaperone 3 | Ofte (30–79 %) | I 1 tilstand |
| BAG5BAG cochaperone 5 | Ofte (30–79 %) | I 1 tilstand |
| CAP2cyclase associated actin cytoskeleton regulatory protein 2 | Ofte (30–79 %) | I 1 tilstand |
| CHD7chromodomain helicase DNA binding protein 7 | Ofte (30–79 %) | I 1 tilstand |
| COL2A1collagen type II alpha 1 chain | Ofte (30–79 %) | I 2 tilstander |
| CRYABcrystallin alpha B | Ofte (30–79 %) | I 1 tilstand |
| CSRP3cysteine and glycine rich protein 3 | Ofte (30–79 %) | I 1 tilstand |
| DESdesmin | Ofte (30–79 %) | I 1 tilstand |
| DGKEdiacylglycerol kinase epsilon | Ofte (30–79 %) | I 1 tilstand |
| DMDdystrophin | Ofte (30–79 %) | I 1 tilstand |
| DOLKdolichol kinase | Ofte (30–79 %) | I 1 tilstand |
| DSG2desmoglein 2 | Ofte (30–79 %) | I 1 tilstand |
| DSPdesmoplakin | Ofte (30–79 %) | I 2 tilstander |
| FHL2four and a half LIM domains 2 | Ofte (30–79 %) | I 1 tilstand |
| FKTNfukutin | Ofte (30–79 %) | I 1 tilstand |
| FLNCfilamin C | Ofte (30–79 %) | I 1 tilstand |
| GATAD1GATA zinc finger domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| GET3guided entry of tail-anchored proteins factor 3, ATPase | Ofte (30–79 %) | I 1 tilstand |
| GNA14G protein subunit alpha 14 | Ofte (30–79 %) | I 1 tilstand |
| GSNgelsolin | Ofte (30–79 %) | I 1 tilstand |
| HAND2heart and neural crest derivatives expressed 2 | Ofte (30–79 %) | I 1 tilstand |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Ofte (30–79 %) | I 1 tilstand |
| HPGD15-hydroxyprostaglandin dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 1 | Ofte (30–79 %) | I 1 tilstand |
| IL2RGinterleukin 2 receptor subunit gamma | Ofte (30–79 %) | I 1 tilstand |
| IL7Rinterleukin 7 receptor | Ofte (30–79 %) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| JPH2junctophilin 2 | Ofte (30–79 %) | I 1 tilstand |
| KIF11kinesin family member 11 | Ofte (30–79 %) | I 1 tilstand |
| LAMA4laminin subunit alpha 4 | Ofte (30–79 %) | I 1 tilstand |
| LDB3LIM domain binding 3 | Ofte (30–79 %) | I 1 tilstand |
| LMNAlamin A/C | Ofte (30–79 %) | I 1 tilstand |
| LMOD2leiomodin 2 | Ofte (30–79 %) | I 1 tilstand |
| LPIN2lipin 2 | Ofte (30–79 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Ofte (30–79 %) | I 1 tilstand |
| MKRN3makorin ring finger protein 3 | Ofte (30–79 %) | I 1 tilstand |
| MPImannose phosphate isomerase | Ofte (30–79 %) | I 2 tilstander |
| MVKmevalonate kinase | Ofte (30–79 %) | I 1 tilstand |
| MYBPC3myosin binding protein C3 | Ofte (30–79 %) | I 1 tilstand |
| MYH6myosin heavy chain 6 | Ofte (30–79 %) | I 1 tilstand |
| MYH7myosin heavy chain 7 | Ofte (30–79 %) | I 1 tilstand |
| MYPNmyopalladin | Ofte (30–79 %) | I 1 tilstand |
| NEU1neuraminidase 1 | Ofte (30–79 %) | I 1 tilstand |
| NEXNnexilin F-actin binding protein | Ofte (30–79 %) | I 1 tilstand |
| NLRP3NLR family pyrin domain containing 3 | Ofte (30–79 %) | I 1 tilstand |
| NPAP1nuclear pore associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| NRAPnebulin related anchoring protein | Ofte (30–79 %) | I 1 tilstand |
| NUDCD3NudC domain containing 3 | Ofte (30–79 %) | I 1 tilstand |
| PLNphospholamban | Ofte (30–79 %) | I 1 tilstand |
| PPCSphosphopantothenoylcysteine synthetase | Ofte (30–79 %) | I 1 tilstand |
| PRDM16PR/SET domain 16 | Ofte (30–79 %) | I 1 tilstand |
| PRF1perforin 1 | Ofte (30–79 %) | I 1 tilstand |
| PSAT1phosphoserine aminotransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| PSEN1presenilin 1 | Ofte (30–79 %) | I 1 tilstand |
| PSEN2presenilin 2 | Ofte (30–79 %) | I 1 tilstand |
| PSMB10proteasome 20S subunit beta 10 | Ofte (30–79 %) | I 1 tilstand |
| PWAR1Prader Willi/Angelman region RNA 1 | Ofte (30–79 %) | I 1 tilstand |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Ofte (30–79 %) | I 1 tilstand |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Ofte (30–79 %) | I 1 tilstand |
| RBM20RNA binding motif protein 20 | Ofte (30–79 %) | I 1 tilstand |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Ofte (30–79 %) | I 1 tilstand |
| RPL3Lribosomal protein L3 like | Ofte (30–79 %) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Ofte (30–79 %) | I 1 tilstand |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Ofte (30–79 %) | I 1 tilstand |
| SGCDsarcoglycan delta | Ofte (30–79 %) | I 1 tilstand |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Ofte (30–79 %) | I 1 tilstand |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Ofte (30–79 %) | I 1 tilstand |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Ofte (30–79 %) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Ofte (30–79 %) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Ofte (30–79 %) | I 1 tilstand |
| STX11syntaxin 11 | Ofte (30–79 %) | I 1 tilstand |
| TAF1ATATA-box binding protein associated factor, RNA polymerase I subunit A | Ofte (30–79 %) | I 1 tilstand |
| TAFAZZINtafazzin, phospholipid-lysophospholipid transacylase | Ofte (30–79 %) | I 1 tilstand |
| TALDO1transaldolase 1 | Ofte (30–79 %) | I 1 tilstand |
| TCAPtitin-cap | Ofte (30–79 %) | I 1 tilstand |
| TMPOthymopoietin | Ofte (30–79 %) | I 1 tilstand |
| TNNC1troponin C1, slow skeletal and cardiac type | Ofte (30–79 %) | I 1 tilstand |
| TNNI3troponin I3, cardiac type | Ofte (30–79 %) | I 1 tilstand |
| TNNT2troponin T2, cardiac type | Ofte (30–79 %) | I 1 tilstand |
| TPM1tropomyosin 1 | Ofte (30–79 %) | I 1 tilstand |
| TPRKBTP53RK binding protein | Ofte (30–79 %) | I 1 tilstand |
| TTNtitin | Ofte (30–79 %) | I 1 tilstand |
| TXNRD2thioredoxin reductase 2 | Ofte (30–79 %) | I 1 tilstand |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Ofte (30–79 %) | I 1 tilstand |
| VCLvinculin | Ofte (30–79 %) | I 1 tilstand |
| VEZF1vascular endothelial zinc finger 1 | Ofte (30–79 %) | I 1 tilstand |
| ABCC6ATP binding cassette subfamily C member 6 | Noen ganger (5–29 %) | I 1 tilstand |
| ACAT1acetyl-CoA acetyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| AGGF1angiogenic factor with G-patch and FHA domains 1 | Noen ganger (5–29 %) | I 1 tilstand |
| B4GALT1beta-1,4-galactosyltransferase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| BMPR1Abone morphogenetic protein receptor type 1A | Noen ganger (5–29 %) | I 1 tilstand |
| CD28CD28 molecule | Noen ganger (5–29 %) | I 2 tilstander |
| CFTRCF transmembrane conductance regulator | Noen ganger (5–29 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Noen ganger (5–29 %) | I 2 tilstander |
| ENGendoglin | Noen ganger (5–29 %) | I 1 tilstand |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| FECHferrochelatase | Noen ganger (5–29 %) | I 2 tilstander |
| GNAQG protein subunit alpha q | Noen ganger (5–29 %) | I 1 tilstand |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Noen ganger (5–29 %) | I 1 tilstand |
| JAG1jagged canonical Notch ligand 1 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| LAMA3laminin subunit alpha 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LAMB3laminin subunit beta 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LAMC2laminin subunit gamma 2 | Noen ganger (5–29 %) | I 1 tilstand |
| LYSTlysosomal trafficking regulator | Noen ganger (5–29 %) | I 1 tilstand |
| MOGSmannosyl-oligosaccharide glucosidase | Noen ganger (5–29 %) | I 1 tilstand |
| PBX1PBX homeobox 1 | Noen ganger (5–29 %) | I 1 tilstand |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Noen ganger (5–29 %) | I 2 tilstander |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Noen ganger (5–29 %) | I 1 tilstand |
| PMM2phosphomannomutase 2 | Noen ganger (5–29 %) | I 1 tilstand |
| RNU7-1RNA, U7 small nuclear 1 | Noen ganger (5–29 %) | I 1 tilstand |
| RYR1ryanodine receptor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Noen ganger (5–29 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| TNFRSF1BTNF receptor superfamily member 1B | Noen ganger (5–29 %) | I 2 tilstander |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ZNFX1zinc finger NFX1-type containing 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ACBD6acyl-CoA binding domain containing 6 | Sjelden (1–4%) | I 1 tilstand |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Sjelden (1–4%) | I 2 tilstander |
| DUOX2dual oxidase 2 | Sjelden (1–4%) | I 1 tilstand |
| GATA1GATA binding protein 1 | Sjelden (1–4%) | I 1 tilstand |
| POLGDNA polymerase gamma, catalytic subunit | Sjelden (1–4%) | I 1 tilstand |
| POLG2DNA polymerase gamma 2, accessory subunit | Sjelden (1–4%) | I 1 tilstand |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sjelden (1–4%) | I 1 tilstand |
| SLC25A4solute carrier family 25 member 4 | Sjelden (1–4%) | I 1 tilstand |
| TSHRthyroid stimulating hormone receptor | Sjelden (1–4%) | I 1 tilstand |
| TWNKtwinkle mtDNA helicase | Sjelden (1–4%) | I 1 tilstand |
| URODuroporphyrinogen decarboxylase | Sjelden (1–4%) | I 1 tilstand |
| UROSuroporphyrinogen III synthase | Sjelden (1–4%) | I 1 tilstand |
| AIPAHR interacting HSP90 co-chaperone | Ikke registrert | I 1 tilstand |
| BLTP1bridge-like lipid transfer protein family member 1 | Ikke registrert | I 1 tilstand |
| BPTFbromodomain PHD finger transcription factor | Ikke registrert | I 1 tilstand |
| BSNDbarttin CLCNK type accessory subunit beta | Ikke registrert | I 1 tilstand |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Ikke registrert | I 1 tilstand |
| CHRNDcholinergic receptor nicotinic delta subunit | Ikke registrert | I 1 tilstand |
| CHRNGcholinergic receptor nicotinic gamma subunit | Ikke registrert | I 1 tilstand |
| CLCNKAchloride voltage-gated channel Ka | Ikke registrert | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Ikke registrert | I 1 tilstand |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Ikke registrert | I 1 tilstand |
| EBPEBP cholestenol delta-isomerase | Ikke registrert | I 1 tilstand |
| EPHB4EPH receptor B4 | Ikke registrert | I 1 tilstand |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Ikke registrert | I 1 tilstand |
| ERCC5ERCC excision repair 5, endonuclease | Ikke registrert | I 1 tilstand |
| FGAfibrinogen alpha chain | Ikke registrert | I 1 tilstand |
| GBE11,4-alpha-glucan branching enzyme 1 | Ikke registrert | I 1 tilstand |
| GLE1GLE1 RNA export mediator | Ikke registrert | I 1 tilstand |
| IL6interleukin 6 | Ikke registrert | I 1 tilstand |
| INPPL1inositol polyphosphate phosphatase like 1 | Ikke registrert | I 1 tilstand |
| KITKIT proto-oncogene, receptor tyrosine kinase | Ikke registrert | I 1 tilstand |
| KRT13keratin 13 | Ikke registrert | I 1 tilstand |
| LAMB2laminin subunit beta 2 | Ikke registrert | I 1 tilstand |
| MKKSMKKS centrosomal shuttling protein | Ikke registrert | I 1 tilstand |
| MRPS22mitochondrial ribosomal protein S22 | Ikke registrert | I 1 tilstand |
| NR2E3nuclear receptor subfamily 2 group E member 3 | Ikke registrert | I 1 tilstand |
| NRASNRAS proto-oncogene, GTPase | Ikke registrert | I 1 tilstand |
| OSGEPO-sialoglycoprotein endopeptidase | Ikke registrert | I 1 tilstand |
| PLD1phospholipase D1 | Ikke registrert | I 1 tilstand |
| SGPL1sphingosine-1-phosphate lyase 1 | Ikke registrert | I 1 tilstand |
| SLC26A2solute carrier family 26 member 2 | Ikke registrert | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Ikke registrert | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | Ikke registrert | I 1 tilstand |
| ZNHIT3zinc finger HIT-type containing 3 | 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
- Fluid around lungs86 gener
- Swelling caused by excess lymph fluid under skin75 gener
- Hydrops fetalis71 gener
- Increased nuchal translucency66 gener
- Fluid accumulation in lower limbs53 gener
- Joint swelling53 gener
- Facial puffiness35 gener
- Brain swelling32 gener
- Excess fluid in lungs30 gener
- Generalized edema18 gener
- Edema of the dorsum of hands16 gener
- Angioedema13 gener
- Corneal stromal edema13 gener
- Peripheral edema11 gener
- Laryngeal edema5 gener
- Fetal skin edema4 gener
- Genital edema4 gener
- Peau d'orange4 gener
- Throat swelling3 gener
- Intestinal edema2 gener
- Tongue edema2 gener
- Hyperkeratosis over edematous areas1 gen
- Hypoproteinemic edema1 gen
- Muscular edema1 gen
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.
Én test. En livstid med svar.
Fra 449 $Gratis frakt · Resultater på 6–8 uker