Version: 8.0.0
Date: Tue Jan 28 2025
2 results
Disease Models: Dnah5<hlb612>/Dnah5<hlb612> [background:] involves: C57BL/6J (Mmu)

tetralogy of Fallot

Disease
Source: DOID:6419
Definition: Not Available

primary ciliary dyskinesia 3

Disease
Source: DOID:0110599
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, ciliary akinesia and variable occurence of situs inversus and has_material_basis_in homozygous or compound heterozygous mutation in the DNAH5 gene on chromosome 5p15.