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
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 31 - 40 of 40 in total
HPO ID HPO Term
HP:0001669 Transposition of the great arteries
HP:0006536 Airway obstruction
HP:0002119 Ventriculomegaly
HP:0012206 Abnormal sperm motility
HP:0011617 Pulmonary situs ambiguus
HP:0100582 Nasal polyposis
HP:0011539 Atrial situs ambiguous
HP:0030680 Abnormal cardiovascular system morphology
HP:0100750 Atelectasis
HP:0011947 Respiratory tract infection
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