OBO ID: DOID:0080266
Term Name: primary ciliary dyskinesia 37 Search Ontology:
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 )
OTHER primary ciliary dyskinesia 37 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DNAH1 Ciliary dyskinesia, primary, 37 617577
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None