OBO ID: DOID:0110606 |
Term Name: | primary ciliary dyskinesia 6 | Search Ontology: | |
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Synonyms: |
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Definition: | A primary ciliary dyskinesia that is characterized by partial outer dynein arm defect and has_material_basis_in mutation in the TXNDC3 gene on the chromosome 7p14.1. (2) | ||
References: |
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Ontology: | Human Disease ( DOID:0110606 ) |
OTHER primary ciliary dyskinesia 6 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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NME8 | ?Ciliary dyskinesia, primary, 6 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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