congenital central hypoventilation syndrome

Summary
Synonym
  • CCHS
  • Ondine curse
  • Ondine syndrome
  • central congenital hypoventilation syndrome
  • congenital central alveolar hypoventilation syndrome
Definition
An autonomic nervous system disease characterized by reduced responsiveness of the respiratory center to carbon dioxide, diminished pupillary light responses, and other symptoms related to defects in the autonomic nervous system and that has_material_basis_in most commonly heterozygous mutation in the PHOX2B gene on chromosome 4p13 and less frequently mutations in the RET, GDNF, EDN3, BDNF, or ASCL1 genes.
Super Class
autonomic nervous system disease autosomal dominant disease physical disorder
External Links
Disease Ontology
DOID:0060731
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 14 of 14 in total
Gene ID Gene Symbol Description Source
54187 NANS N-acetylneuraminate synthase
55556 ENOSF1 enolase superfamily member 1
79158 GNPTAB N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
81031 SLC2A10 solute carrier family 2 member 10

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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