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Human Disease and Mouse Model Detail
Human Disease Central Hypoventilation Syndrome, Congenital; CCHS
OMIM ID: 209880
Human Phenotype Ontology associations
Synonyms Autonomic Control, Congenital Failure of
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PHOX2B* Phox2b* View 1 model HomoloGene and HGNC
     TLX3 Tlx3* View 1 model HomoloGene and HGNC
     ASCL1* Ascl1   HomoloGene and HGNC
BDNF* Bdnf   HomoloGene and HGNC
EDN3* Edn3   HomoloGene and HGNC
GDNF* Gdnf   HomoloGene and HGNC
RET* Ret   HomoloGene and HGNC
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory