primary ciliary dyskinesia 5

Summary
Synonym
  • CILD5
  • primary ciliary dyskinesia 5 without situs inversus
Definition
A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has_material_basis_in homozygous mutation in the HYDIN gene on chromosome 16q22.
Super Class
primary ciliary dyskinesia
External Links
Disease Ontology
DOID:0110617
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
54768 HYDIN HYDIN axonemal central pair apparatus protein
The Human Phenotype Ontology
Displaying entries 21 - 30 of 40 in total
HPO ID HPO Term
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
HP:0001669 Transposition of the great arteries
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