About   Help   FAQ
Disease Ontology Browser
congenital central hypoventilation syndrome (DOID:0060731)
Alliance: disease page
Synonyms: CCHS; central congenital hypoventilation syndrome; congenital central alveolar hypoventilation syndrome; Ondine curse; Ondine syndrome
Alt IDs: OMIM:209880, ICD10CM:G47.3, MESH:C536209, ORDO:661
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.

Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory