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Human Disease and Mouse Model Detail
Human Disease Cowchock Syndrome; COWCK
OMIM ID: 310490
Synonyms Charcot-Marie-Tooth Disease; Charcot-Marie-Tooth Disease with Deafness and Mental Retardation; Charcot-Marie-Tooth Disease, X-Linked Recessive, 4; CMTX4; NADMR; Neuropathy, Axonal Motor-Sensory, with Deafness and Mental Retardation; NAMSD
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

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 5.22
The Jackson Laboratory