17q12 Kennisbankdeletion syndrome · static snapshot
Alle inhoud is verzameld van openbare internetbronnen en verwerkt met hulp van AI/LLM-software. Deze website is alleen informatief — trek er geen conclusies uit; controleer bij de originele bronnen. Volledige disclaimer
Gen–kenmerk-koppeling Klachten & kenmerken 10 ondersteunende bronnen vertrouwen 97% nieuwheid 54%

ZNHIT3 komt in 10 bronnen samen met lever en galblaas voor

In het verzamelde corpus komt het gen ZNHIT3 in 10 onafhankelijke documenten samen met lever en galblaas voor. Associatiesterkte 0.09..

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 gisteren. Dedup-sleutel assoc:ZNHIT3: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 (4 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:…
…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 (33)

DocumentBronGepubliceerdGezienRelevantie
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
Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 gisteren 1.00
Decreased T helper 1 cell function underlies recurrent sinopulmonar... pmc 2025-01-01 gisteren 1.00
Case-based learning: a case of maturity-onset diabetes of the young... pmc 2025-01-01 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
17q12 Microdeletion Syndrome Initially Presenting with Tremor in Ma... 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
Reversed cortico-medullary differentiation in kidneys on fetal magn... pmc 2025-01-01 gisteren 1.00
Prenatally diagnosed 17q12 microdeletion syndrome with a novel asso... pubmed 2012-01-01 gisteren 1.00
Case Report: Nephrocalcinosis from pancreatic hypoplasia in HNF1B d... pmc 2026-01-01 gisteren 1.00
Unraveling the Genetic Mysteries of Müllerian Anomalies: Research A... 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
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
17q12 deletion syndrome presenting with chronic pancreatitis: a case report pmc 2026-01-01 gisteren 1.00
A familial case report of 17q12 recurrent deletion syndrome: clinic... 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
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
[Clinical and genetic analysis of a fetus with 17q12 microdeletion ... pubmed 2023-06-10 gisteren 1.00
Heterozygous ZNHIT3 variants within the 17q12 recurrent deletion re... pubmed 2024-08-01 gisteren 1.00
PMC12903773 local_files - gisteren 1.00