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Human Disease and Mouse Model Detail
Human Disease Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis;
OMIM ID: 602066
Synonyms ICCA; ICCA Syndrome; Infantile Convulsions and Paroxysmal Choreoathetosis, Familial; Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions; PKD/IC
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
     PRRT2* Prrt2   HomoloGene

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 6.02
The Jackson Laboratory