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DOID:0110610 - primary ciliary dyskinesia 34
Disease Ontology 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.
Synonyms: CILD34, primary ciliary dyskinesia 34 without situs inversus
Xenbase Genes

MONDO:0014909 - primary ciliary dyskinesia 34 |
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)