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DOID:0110606 - primary ciliary dyskinesia 6
Disease Ontology 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.
Synonyms: CILD6,
Xenbase Genes :
MONDO:0012571 - primary ciliary dyskinesia 6 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
primary ciliary dyskinesia (is_a)