17q12 Kennisbankdeletion syndrome · static snapshot
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Gen–kenmerk-koppeling Klachten & kenmerken 134 ondersteunende bronnen vertrouwen 97% nieuwheid 75%

HNF1B komt in 76 bronnen samen met lever en galblaas voor

In het verzamelde corpus komt het gen HNF1B in 76 onafhankelijke documenten samen met lever en galblaas voor. Associatiesterkte 0.43..

Hoe dit tot stand kwam

Gelijktijdig voorkomen is een *waarneming over de literatuur*, geen bewijs van oorzakelijkheid: het zegt dat deze onderwerpen in onze bronnen samen worden besproken.

Gegenereerd 2026-11-13, laatst gewijzigd vandaag. Dedup-sleutel assoc:HNF1B:hepatic. De engine controleert dit inzicht bij elke analyse opnieuw; als meer bronnen het eens zijn, stijgen zijn onderbouwing en vertrouwen en verschijnt het opnieuw als “nieuw”.

Bewijs (5 citaten)

…ology, Professor of Internal Medicine, Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, Saint Louis University Liver Center, 3635 Vista Avenue at Grand Boulevard, St. Louis, MO 63110-0250. E-mail: baconbr@slu.edu; fax: 314-577-8125 . Potential conflict of interest:…
…ical syndrome (kidney and urogenital malformations, maturity-onset diabetes of the young, exocrine pancreatic insufficiency) and to an underdiagnosed liver involvement. Differently from HNF1A , the correlation between hepatocellular carcinoma (HCC) and germline HNF1B deficiency has been poorly evaluated.…
…irst case, a 29-year-old woman, presented with diabetes, hypertension, bilateral renal cysts, mild chronic kidney disease (CKD), hypomagnesemia, mild liver enzyme elevations, and a complex Müllerian anomaly requiring surgical correction. She has maintained excellent metabolic control on metformin alone,…
…lestasis was rapidly resolved with hormone therapy. Genetic analysis showed a de novo 17q chromosome deletion, including the HNF1β gene implicated in liver damage, and this was considered causative of the complex clinical phenotype. Our case highlights the relationship between congenital hypopituitarism…
…hepatic transcriptional regulators but has since been recognized as master coordinators of metabolic homeostasis across multiple organs including the liver, kidneys, and pancreas(16-18). As a key hub in the regulation of systemic lipid homeostasis, HNF-1 family exerts biological functions by coordinating…

Ondersteunende documenten (47)

DocumentBronGepubliceerdGezienRelevantie
A Simple Bioreactor-Based Method to Generate Kidney Organoids from ... pubmed 2018-08-14 gisteren 0.74
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 gisteren 1.00
Atypical presentation of HNF1β gene mutation mimicking type 2 diabe... pmc 2025-01-01 gisteren 1.00
A Case of 17q12 Microdeletion Syndrome in a MODY5 Type Diabetes wit... pmc 2024-01-01 gisteren 1.00
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and... pmc 2024-01-01 gisteren 1.00
A Korean Family Presenting with Renal Cysts and Maturity-Onset Diab... pmc 2024-01-01 gisteren 1.00
Monogenic Defects of Beta Cell Function: From Clinical Suspicion to... pmc 2024-01-01 gisteren 0.45
HNF1B Transcription Factor: Key Regulator in Renal Physiology and P... pmc 2024-01-01 gisteren 1.00
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deleti... pmc 2024-01-01 gisteren 1.00
School level of children carrying a HNF1B variant or a deletion. pubmed 2020-01-01 gisteren 1.00
The Clinical Characteristics and Gene Mutations of Maturity-Onset D... pubmed 2022-01-01 gisteren 1.00
New case of syncytial giant-cell variant of hepatocellular carcinom... pubmed 2022-12-01 gisteren 1.00
Hepatocyte nuclear factor 1B deletion, but not intragenic mutation,... pubmed 2024-01-01 gisteren 1.00
Large Kidney Cysts in HNF1B Nephropathy Mimicking Autosomal Dominan... pubmed 2024-01-01 gisteren 1.00
Monogenic Etiologies of Kidney Cysts in the Pediatric Population: A... pubmed 2026-06-01 gisteren 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pubmed 2026-01-01 gisteren 1.00
From Exome to Optical Mapping: Resolving a Complex 17q12 Rearrangem... pubmed 2026-10-09 gisteren 1.00
Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 gisteren 1.00
Severe neonatal cholestasis in HNF1β deficiency: a case report and ... pmc 2025-01-01 gisteren 1.00
Distinct chromosome abnormality patterns for differential diagnosis... pmc 2025-01-01 gisteren 1.00
Diabetes associated with HNF1B: beyond Occam’s razor—A case report pmc 2025-01-01 gisteren 1.00
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pmc 2025-01-01 gisteren 1.00
MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Pren... pmc 2025-01-01 gisteren 1.00
Double Common Bile Duct Associated With Choledochal Cyst: A Rare De... pmc 2025-01-01 gisteren 1.00
HNF1β Gene Mutation Leading to a MODY5 With Renal Dysplasia: A Case Report pmc 2025-01-01 gisteren 1.00
Application of array-comparative genomic hybridization in tetralogy... pubmed 2016-12-01 gisteren 1.00
Hepatocyte nuclear factor 1 in renal lipid metabolism: molecular me... pmc 2025-01-01 gisteren 1.00
From mutation to symptoms: a multi-center study on HNF1B -related n... pmc 2025-01-01 gisteren 1.00
HNF1B variant without hyperglycaemia as a cause of isolated profoun... pubmed 2023-02-09 gisteren 1.00
The Genetic Landscape and Precision Medicine in Neonatal Diabetes M... pmc 2026-01-01 gisteren 1.00
A complex microdeletion 17q12 phenotype in a patient with recurrent... pubmed 2012-05-14 gisteren 1.00
Case Report: Nephrocalcinosis from pancreatic hypoplasia in HNF1B d... pmc 2026-01-01 gisteren 1.00
Pediatric Hepatocyte Nuclear Factor 1B ( HNF1B ) Disease: Diabetes ... pmc 2025-01-01 gisteren 1.00
The Importance of Molecular Testing in the Diagnosis of Genetic Syn... pmc 2026-01-01 gisteren 1.00
A novel inversion at 17q12 disrupting HNF1B gene in a patient with ... pmc 2026-01-01 gisteren 1.00
Hepatic dysfunction, hyperuricemia, and multiple renal cysts in ado... pmc 2026-01-01 gisteren 1.00
Transient neonatal diabetes mellitus as an early diagnostic clue to... pmc 2026-01-01 gisteren 1.00
Chromosome 17q12 deletion, including HNF1B presenting with recurren... pmc 2026-01-01 gisteren 1.00
Functional validation of a non-canonical HNF1B splice-site variant in MODY5 pmc 2026-01-01 gisteren 1.00
Molecular impact of a novel HNF1B missense variant in childhood-ons... pmc 2026-01-01 gisteren 1.00
HNF1B-MODY in the Norwegian MODY Registry and the Norwegian Childho... pmc 2026-01-01 gisteren 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pmc 2026-01-01 gisteren 1.00
HNF1B -related disease: developmental origins, molecular mechanisms... pmc 2026-01-01 gisteren 1.00
Clinical Spectrum and Early Renal Functional Variability in a Natio... pmc 2026-01-01 gisteren 1.00
Precision Medicine in Pediatric Nephrology: From Shared Clinical Ph... pmc 2026-01-01 gisteren 1.00
Genetic Insights into Pediatric Polycystic Kidney Disease and Overl... pmc 2026-01-01 gisteren 1.00
PMC12903773 local_files - gisteren 1.00