primary ciliary dyskinesia 10

Summary
Synonym
  • CILD10
  • primary ciliary dyskinesia 10 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by outer and inner dynein arm absence, chronic otitis media, sinusitis, recurrent pneumonia and variable occurrence of situs inversus and has_material_basis_in homozygous mutation in the KTU gene on chromosome 14q21.
Super Class
primary ciliary dyskinesia
External Links
Disease Ontology
DOID:0110612
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
55172 DNAAF2 dynein axonemal assembly factor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
109065 Dnaaf2 dynein, axonemal assembly factor 2
The Human Phenotype Ontology
Displaying entries 21 - 30 of 40 in total
HPO ID HPO Term
HP:0002643 Neonatal respiratory distress
HP:0001217 Clubbing
HP:0005301 Persistent left superior vena cava
HP:0002011 Morphological central nervous system abnormality
HP:0010772 Anomalous pulmonary venous return
HP:0001719 Double outlet right ventricle
HP:0002566 Intestinal malrotation
HP:0011274 Recurrent mycobacterial infections
HP:0001746 Asplenia
HP:0002878 Respiratory failure
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: August 19, 2024