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Human Disease and Mouse Model Detail
Human Disease Cowchock Syndrome; COWCK
OMIM ID: 310490
Human Phenotype Ontology associations
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
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
     AIFM1* Aifm1   HomoloGene and HGNC

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