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Human Disease and Mouse Model Detail
Human Disease Chudley-Mccullough Syndrome; CMCS
OMIM ID: 604213
Human Phenotype Ontology associations
Synonyms Deafness, Autosomal Recessive 82, Formerly; DFNB82, FORMERLY; Deafness, Sensorineural, with Partial Agenesis of the Corpus Callosum and Arachnoid Cysts
View all models View ALL (1) 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
     GPSM2* Gpsm2* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (1)

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
11/22/2016
MGI 6.06
The Jackson Laboratory