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General Information
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| Term |
primary ciliary dyskinesia 34 |
ID (Ontology) |
DOID:0110610 (Human Disease) |
| Definition |
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with childhood onset of recurrent sinopulmonary infections and male infertility and has_material_basis_in homozygous mutation in the DNAJB13 gene on chromosome 11q13. |
| Also Known As |
"CILD34" ; "primary ciliary dyskinesia 34 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 34 | 3 | for disease ribbon | primary ciliary dyskinesia 34 | 3 | model of | primary ciliary dyskinesia 34 | 3 |
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