Wicipedia

syndrom neffrotig

Creu erthygl

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Human disease

Adnoddau allanol

dynodwr Freebase
/m/01n597[1]
dynodwr LCAuth
sh85090863[2]

enwyd fel: Nephrotic syndrome

Experimental Factor Ontology ID
0004255[3]
dynodwr Quora
Nephrotic-Syndrome[4]
eMedicine ID
244631
982920
dynodwr KEGG
H01657
Baidu Tieba name
肾病综合症

nifer o weithiau: 4,118,171

pwynt mewn amser: 3 Ebrill 2023

OpenAlex ID
C2778930706[5]
C2910035153[5]
Disease Ontology ID
DOID:1184[6]
Elhuyar ZTH ID
028549
WikiProjectMed ID
Nephrotic syndrome
MedlinePlus ID
000490
Cod MeSH
C12.950.419.630.643
C12.050.351.968.419.630.643
C12.200.777.419.630.643
dynodwr NDL
00568067
Mondo ID
MONDO_0005377
Human Phenotype Ontology ID
HP:0000100[7]
dynodwr Encyclopædia Britannica Online
science/nephrotic-syndrome

enwyd fel: nephrotic syndrome

ICD-11 ID (MMS)
GB41

enwyd fel: Nephrotic syndrome

dynodwr JSTOR (pwnc)
nephrotic-syndrome
Great Russian Encyclopedia Online ID (old version)
2264072

enwyd fel: НЕФРОТИЧЕСКИЙ СИНДРОМ

WikiSkripta article ID
4700
UMLS CUI
C0027726[6][7]
C0027726[8]

mapping relation type: exact match

ICD-11 (foundation)
1184209951
ICD-10-CM
N04[6][8]
dynodwr yn thesawrws y BNCF
46685[9]
dynodwr NKC
ph1141786[10]

enwyd fel: nefrotický syndrom

dynodwr MeSH
D009404[8]

enwyd fel: Nephrotic Syndrome

mapping relation type: exact match

ID NALT
54646
dynodwr BnF
12520979g[2]

enwyd fel: Syndrome néphrotique

DiseasesDB
8905
National Library of Israel J9U ID
987007565632005171[11]

enghraifft o'r canlynol

clefyd prin
dosbarth o glefyd

isddosbarth o'r canlynol

nephrosis[6]
clefyd

arbenigedd meddygol

nephrology

symtomau

proteinuria[12]

nodwedd o'r endid: severe

hypoalbuminemia[12]

cyffuriau a ddefnyddir

clortalidon[13]
cylchothiasid[14]
cwinethason[15]
hydrofflwmethiasid[16]
bwmetanid[17]
bensthiasid[18]
cycloffosffamid[19]
methyclothiasid[20]
metolason[21]
hydroclorothiasid[22]
ffwrosemid[23]
indapamid[24]
asid etacrynig[25]
bendrofflwmethiasid[26]
clorothiasid sodiwm[27]
triclormethiasid[28]
polythiasid[29]
torasemid[30]
ethacrynate sodium[31]
prednison[32]
rituximab[32]
ciclosporin[32]
mycophenolate mofetil[32]
prednisolon[32]
methylprednisolon[32]
tacrolimws[32]
clorothiasid sodiwm[33]

cadarnhawyd gan: Food and Drug Administration

dyddiad neu amser cychwyn: 2 Hydref 1958

cycloffosffamid[34]

cadarnhawyd gan: Food and Drug Administration

dyddiad neu amser cychwyn: 12 Ebrill 1960

genetic association

GPC5[35]

dull penderfynu: genome-wide association study, TAS

LAMB2[36]
COQ8B[37][38]
ARHGDIA[39]
DGKE[40]
WT1[41]
NPHS2[42]
NPHS1[43]
PLCE1[44]
PTPRO[45]
EMP2[46]
SGPL1[47]

disgrifiwyd gan y ffynhonnell

Gwyddoniadur Sofiet-Armeniaidd

ar restr sylw'r prosiect Wikimedia

Wicipedia:WiciBrosiect Meddygaeth

ICD-9-CM

581[6][8]
581.9[8]

Thesawrws NCI

C34845[6]
C34845[8]

mapping relation type: exact match

cysyniad o'r un fath

http://purl.obolibrary.org/obo/DOID_1184[6]
http://identifiers.org/doid/DOID:1184[48]
http://purl.obolibrary.org/obo/HP_0000100[7]

yn wahanol i

nephritic syndrome

Cyfeiriadau

  1. ↑ Freebase Data Dumps, 28 Hydref 2013
  2. ↑ 2.0 2.1 Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=46685, 16 Mehefin 2021
  3. ↑ inferred by common MONDO mappings on source and on Wikidata
  4. ↑ Quora
  5. ↑ 5.0 5.1 OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  6. ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 Disease Ontology, 15 Mai 2019, DOID:1184
  7. ↑ 7.0 7.1 7.2 Human Phenotype Ontology release 2018-03-08, 8 Hydref 2018, HP:0000100
  8. ↑ 8.0 8.1 8.2 8.3 8.4 8.5 Monarch Disease Ontology release 2018-06-29, 4 Awst 2018, MONDO_0005377
  9. ↑ National Central Library of Florence
  10. ↑ ph1141786, 24 Chwefror 2022, Národní autority České republiky
  11. ↑ Llyfrgell Genedlaethol Israel
  12. ↑ 12.0 12.1 https://icd.who.int/dev11/f/en#/http%3a%2f%2fid.who.int%2ficd%2fentity%2f1184209951
  13. ↑ N0000146240, 13 Rhagfyr 2016, NDF-RT, Saesneg
  14. ↑ N0000145889, 13 Rhagfyr 2016, NDF-RT, Saesneg
  15. ↑ N0000146252, 13 Rhagfyr 2016, NDF-RT, Saesneg
  16. ↑ N0000146480, 13 Rhagfyr 2016, NDF-RT, Saesneg
  17. ↑ N0000146155, 13 Rhagfyr 2016, NDF-RT, Saesneg
  18. ↑ N0000146743, 13 Rhagfyr 2016, NDF-RT, Saesneg
  19. ↑ N0000146452, 13 Rhagfyr 2016, NDF-RT, Saesneg
  20. ↑ N0000146766, 13 Rhagfyr 2016, NDF-RT, Saesneg
  21. ↑ N0000146498, 13 Rhagfyr 2016, NDF-RT, Saesneg
  22. ↑ N0000145995, 13 Rhagfyr 2016, NDF-RT, Saesneg
  23. ↑ N0000146188, 13 Rhagfyr 2016, NDF-RT, Saesneg
  24. ↑ N0000147050, 13 Rhagfyr 2016, NDF-RT, Saesneg
  25. ↑ N0000146283, 13 Rhagfyr 2016, NDF-RT, Saesneg
  26. ↑ N0000145992, 13 Rhagfyr 2016, NDF-RT, Saesneg
  27. ↑ N0000146099, 13 Rhagfyr 2016, NDF-RT, Saesneg
  28. ↑ N0000146925, 13 Rhagfyr 2016, NDF-RT, Saesneg
  29. ↑ N0000146940, 13 Rhagfyr 2016, NDF-RT, Saesneg
  30. ↑ N0000148359, 13 Rhagfyr 2016, NDF-RT, Saesneg
  31. ↑ N0000146284, 13 Rhagfyr 2016, NDF-RT, Saesneg
  32. ↑ 32.0 32.1 32.2 32.3 32.4 32.5 32.6 Drug Indications Extracted from FAERS, 2 Hydref 2018
  33. ↑ Inxight: Drugs Database, 2 Tachwedd 2018, https://drugs.ncats.io/drug/77W477J15H, https://www.drugs.com/pro/diuril-injection.html
  34. ↑ Inxight: Drugs Database, 2 Tachwedd 2018, https://drugs.ncats.io/drug/6UXW23996M, http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/012141s090,012142s112lbl.pdf
  35. ↑ Phenocarta, Common variation in GPC5 is associated with acquired nephrotic syndrome, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1184&ncbiId=2262, http://www.genome.gov/gwastudies/index.cfm?gene=GPC5, 25 Mai 2020
  36. ↑ Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
  37. ↑ ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
  38. ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000123815/EFO_0004255, inferred from an Open Targets association score over 0.7
  39. ↑ ARHGDIA: a novel gene implicated in nephrotic syndrome
  40. ↑ DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
  41. ↑ Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
  42. ↑ NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
  43. ↑ Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome
  44. ↑ Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
  45. ↑ Disruption of PTPRO causes childhood-onset nephrotic syndrome
  46. ↑ Mutations in EMP2 cause childhood-onset nephrotic syndrome
  47. ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000166224/EFO_0004255, inferred from an Open Targets association score over 0.7
  48. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233
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