primary ciliary dyskinesia 23

Summary
Synonym
  • CILD23
  • primary ciliary dyskinesia 23 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, respiratory distress and recurrent upper and lower airway infections, and variable occurence of situs inversus and has_material_basis_in homozygous or compound heterozygous mutation in the ARMC4 gene on chromosome 10p.
Super Class
primary ciliary dyskinesia
Disease Ontology
DOID:0110609
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
55130 ODAD2 outer dynein arm docking complex subunit 2
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