Osebold-Remondini syndrome
MONDO:0007219Mondo
Findings
No curated finding names Osebold-Remondini syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A brachymesophalangy with mesomelic short limbs, and carpal and tarsal bone abnormalities. In general, the affected individuals are of slightly short stature and normal intelligence. The syndrome has been described in a kindred with seven affected members from three generations. Transmission appears to be autosomal dominant.
Definition from the Mondo Disease Ontology (MONDO:0007219), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
4 names
Resolves to: Osebold-Remondini syndrome
- Also called
- BDA6brachydactyly type A6brachydactyly, type A6brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities