Search Ontology:
Human Disease

primary ciliary dyskinesia 37

Term ID
DOID:0080266
Synonyms
Definition
A primary ciliary dyskinesia that has_material_basis_in homozygous mutation in the DNAH1 gene on chromosome 3p21. https://pubmed.ncbi.nlm.nih.gov/25927852/
References
Ontology
Human Disease   ( DOID:0080266 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models