Advanced search

Combine gene, variant, phenotype, region and year filters

Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

Transparent by designEvery result links extracted entities to its source sentence and publication identifier.
About your search

ADAMTS13 and renal failure are reported together in 1 article.

HGNC
HGNC:1366
8articles
8mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype

Renal failure

523articles
523mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

Recurrent C3 Glomerulonephritis with an ADAMTS 13 Gene Variant: A Case Report and Literature Review.

PMID 35946293 | DOI 10.4103/1319-2442.352441 · Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia · 2021 · 2 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneADAMTS13“After 19 months, the patient experienced recurrent C3GN (rC3GN) that involved a variant of unknown significance in the ADAMTS13 gene.”0.98hgnc_dict_v1
phenotyperenal failure“A 28-year-old male with end-stage renal disease caused by C3GN underwent renal transplantation.”0.93phenotype_alias_lexicon_v2