Gene + body-part link
What it can look like
40 supporting sources
confidence 97%
novelty 62%
The gene HNF1B shows up in 30 stories together with bones and arms or legs
We read 30 stories that talk about both the gene HNF1B and bones and arms or legs. That does not prove one causes the other, but they keep showing up together.
How this was derived
This is about what shows up together in the articles. It is not proof that one thing causes the other.
Generated 2026-11-13, last changed
today. Dedup key assoc:HNF1B:musculoskeletal.
The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.
Evidence (4 quotes)
Genetic Susceptibility to Sport-Related Muscle Injuries: Insights from the Literature and Novel Gene Candidates
peer_reviewed
· published 2025-01-01
· live page
Abstract Physical activity is widely recognized for its health benefits; however, it also increases the risk of musculoskeletal soft tissue injuries, with muscle-related cases constituting a considerable proportion. These injuries impair well-being, athletic performance, and c…
In-Depth Phenotyping of PIGW -Related Disease and Its Role in 17q12 Genomic Disorder
peer_reviewed
· published 2024-01-01
· live page
…bsence of alternative etiology and the already described widely spaced teeth [ 10 , 14 ], tooth agenesis could be a new finding. An additional unique skeletal finding was a duplicated hallux found in P4. Skeletal and extremity anomalies were frequent in the PIGW cohort. Some fetuses presented shortening of…
Delineation of the Genetic Architecture and Clinical Polymorphism of 3q29 Duplication Syndrome: A Review of the Literature and a Report of Two Novel Patients With Single‐Gene BDH1 Duplications
peer_reviewed
· published 2024-01-01
· live page
…ominent supraorbital ridges, wide nasal bridge, cleft ala nasi, microretrognathia, gothic palate, short neck, funnel chest, nipple hypertelorism, and flat feet. A single‐gene duplication of the BDH1 gene, a candidate gene for chromosome 3q29 duplication syndrome (OMIM 611936), was detected in Patient 3.1 (ar…
Precision Medicine in Pediatric Nephrology: From Shared Clinical Phenotypes to Genotype-Guided Diagnosis and Management
peer_reviewed
· published 2026-01-01
· live page
…ease or kidney failure, consanguinity, and extrarenal findings. Assessment of hearing, vision, hematologic, neurodevelopmental, hepatopancreatic, and skeletal or dysmorphic features may reveal a syndromic diagnosis not apparent from the kidney phenotype alone [ 1 , 2 , 3 ]. Encoding granular observations wi…