OBO ID: DOID:0110600
Term Name: primary ciliary dyskinesia 29 Search Ontology:
Synonyms:
  • CILD29
  • primary ciliary dyskinesia 29 without situs inversus
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with oligocilia and early childhood onset of recurrent respiratory infections, and has_material_basis_in homozygous or compound heterozygous mutation in the CCNO gene on chromosome 5p15. (2)
References:
Ontology: Human Disease   ( DOID:0110600 )
Relationships
is a type of:
OTHER primary ciliary dyskinesia 29 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CCNO Ciliary dyskinesia, primary, 29
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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