primary ciliary dyskinesia 14

Summary
Synonym
  • CILD14
  • primary ciliary dyskinesia 14 with or without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with inner dynein arm defect and axonemal disorganization, chronic upper and lower airway infections, and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC39 gene on chromosome 3q26.
Super Class
primary ciliary dyskinesia
External Links
Disease Ontology
DOID:0110598
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
339829 CCDC39 coiled-coil domain 39 molecular ruler complex subunit
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

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024