syndrom neffrotig
Gwedd
Human disease
enghraifft o'r canlynol
clefyd prin
dosbarth o glefyd
arbenigedd meddygol
nephrology
cyffuriau a ddefnyddir
ethacrynate sodium[31]
rituximab[32]
mycophenolate mofetil[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
disgrifiwyd gan y ffynhonnell
Gwyddoniadur Sofiet-Armeniaidd
ar restr sylw'r prosiect Wikimedia
cysyniad o'r un fath
yn wahanol i
nephritic syndrome
Cyfeiriadau
- ↑ Freebase Data Dumps, 28 Hydref 2013
- ↑ 2.0 2.1 Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=46685, 16 Mehefin 2021
- ↑ inferred by common MONDO mappings on source and on Wikidata
- ↑ Quora
- ↑ 5.0 5.1 OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ 6.0 6.1 6.2 6.3 6.4 6.5 6.6 Disease Ontology, 15 Mai 2019, DOID:1184
- ↑ 7.0 7.1 7.2 Human Phenotype Ontology release 2018-03-08, 8 Hydref 2018, HP:0000100
- ↑ 8.0 8.1 8.2 8.3 8.4 8.5 Monarch Disease Ontology release 2018-06-29, 4 Awst 2018, MONDO_0005377
- ↑ National Central Library of Florence
- ↑ ph1141786, 24 Chwefror 2022, Národní autority České republiky
- ↑ Llyfrgell Genedlaethol Israel
- ↑ 12.0 12.1 https://icd.who.int/dev11/f/en#/http%3a%2f%2fid.who.int%2ficd%2fentity%2f1184209951
- ↑ N0000146240, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000145889, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146252, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146480, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146155, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146743, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146452, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146766, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146498, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000145995, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146188, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000147050, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146283, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000145992, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146099, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146925, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146940, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000148359, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ N0000146284, 13 Rhagfyr 2016, NDF-RT, Saesneg
- ↑ 32.0 32.1 32.2 32.3 32.4 32.5 32.6 Drug Indications Extracted from FAERS, 2 Hydref 2018
- ↑ Inxight: Drugs Database, 2 Tachwedd 2018, https://drugs.ncats.io/drug/77W477J15H, https://www.drugs.com/pro/diuril-injection.html
- ↑ Inxight: Drugs Database, 2 Tachwedd 2018, https://drugs.ncats.io/drug/6UXW23996M, http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/012141s090,012142s112lbl.pdf
- ↑ 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
- ↑ Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders
- ↑ ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
- ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000123815/EFO_0004255, inferred from an Open Targets association score over 0.7
- ↑ ARHGDIA: a novel gene implicated in nephrotic syndrome
- ↑ DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN
- ↑ 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
- ↑ NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
- ↑ Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome
- ↑ Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
- ↑ Disruption of PTPRO causes childhood-onset nephrotic syndrome
- ↑ Mutations in EMP2 cause childhood-onset nephrotic syndrome
- ↑ Open Targets Platform, 24 Awst 2023, https://platform.opentargets.org/evidence/ENSG00000166224/EFO_0004255, inferred from an Open Targets association score over 0.7
- ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233