primary ciliary dyskinesia 25

Summary
Synonym
  • CILD25
  • primary ciliary dyskinesia 25 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner and outer dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, decreased fertility and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the DYX1C1 gene on chromosome 15q21.
Super Class
primary ciliary dyskinesia
External Links
Disease Ontology
DOID:0110615
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
161582 DNAAF4 dynein axonemal assembly factor 4
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: August 19, 2024