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General Information
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| Term |
primary ciliary dyskinesia 25 |
ID (Ontology) |
DOID:0110615 (Human Disease) |
| Definition |
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, decreased fertility and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the DYX1C1 gene on chromosome 15q21. |
| Also Known As |
"CILD25" ; "primary ciliary dyskinesia 25 with or without situs inversus" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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primary ciliary dyskinesia 25 | 1 | for disease ribbon | primary ciliary dyskinesia 25 | 1 | model of | primary ciliary dyskinesia 25 | 1 |
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Relationships