primary ciliary dyskinesia 14

Summary
Synonym
  • CILD14
  • primary ciliary dyskinesia 14 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner dynein arm defect and axonemal disorganization, chronic upper and lower airway infections, and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC39 gene on chromosome 3q26.
Super Class
primary ciliary dyskinesia
Disease Ontology
DOID:0110598
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
339829 CCDC39 coiled-coil domain 39 molecular ruler complex subunit
The Human Phenotype Ontology
Displaying entries 11 - 20 of 40 in total
HPO ID HPO Term
HP:0001748 Polysplenia
HP:0011535 Abnormal atrial arrangement
HP:0001696 Situs inversus totalis
HP:0008222 Female infertility
HP:0002257 Chronic rhinitis
HP:0001627 Abnormal heart morphology
HP:0005425 Recurrent sinopulmonary infections
HP:0002110 Bronchiectasis
HP:0011109 Chronic sinusitis
HP:0001742 Nasal congestion
Displaying 1 entry
Gene ID Gene Symbol Description
6674 SPAG1 sperm associated antigen 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024