primary ciliary dyskinesia 28

Summary
Synonym
  • CILD28
  • primary ciliary dyskinesia 28 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer and inner dynein arm defect, recurrent upper and lower airway disease, bronchiectasis, and decreased fertility and has_material_basis_in homozygous or compound heterozygous mutation in the SPAG1 gene on chromosome 8q22.
Super Class
primary ciliary dyskinesia
External Links
Disease Ontology
DOID:0110607
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6674 SPAG1 sperm associated antigen 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 48 in total
HPO ID HPO Term
HP:0000389 Chronic otitis media
HP:0000750 Delayed speech and language development
HP:0000238 Hydrocephalus
HP:0000405 Conductive hearing impairment
HP:0000119 Abnormality of the genitourinary system
HP:0000510 Rod-cone dystrophy
HP:0000365 Hearing impairment
HP:0000924 Abnormality of the skeletal system
HP:0000403 Recurrent otitis media
HP:0003251 Male infertility
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