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 )
- is a type of
-
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Genes Involved
Zebrafish Models