primary ciliary dyskinesia 30

Summary
Synonym
  • CILD30
  • primary ciliary dyskinesia 30 without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, nasal blockages, polyps, otitis media, and variable occurence of laterality defects and has_material_basis_in homozygous mutation in the CCDC151 gene on chromosome 19p13.
Super Class
primary ciliary dyskinesia
Disease Ontology
DOID:0110624
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
115948 ODAD3 outer dynein arm docking complex subunit 3
The Human Phenotype Ontology
Displaying entries 21 - 30 of 40 in total
HPO ID HPO Term
HP:0000924 Abnormality of the skeletal system
HP:0003251 Male infertility
HP:0001748 Polysplenia
HP:0008222 Female infertility
HP:0001696 Situs inversus totalis
HP:0002257 Chronic rhinitis
HP:0011109 Chronic sinusitis
HP:0001742 Nasal congestion
HP:0002643 Neonatal respiratory distress
HP:0001627 Abnormal heart morphology
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