Version: 8.0.0Date: Tue Jan 28 2025
Disease
Source: DOID:0050592
Definition: A bone development disease characterized by skeletal abnormalities and resulting in difficulty in breathing caused by mutations that result in ciliopathy.
Genes: DYNC2LI1 (Hsa)...Dync2li1 (Mmu)...Dync2li1 (Rno)...dync2li1 (Dre)...dync2li1 (Xtr)