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Human Disease and Mouse Model Detail
Human Disease Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1;
OMIM ID: 603387
Synonyms Meg-Pmg-Megacc Syndrome; Megalencephaly, Mega Corpus Callosum, and Complete Lack of Motor Development; Megalencephaly, Polymicrogyria, Mega Corpus Callosum Syndrome; MPPH; Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome; Mpph1
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
     PIK3R2* Pik3r2   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 6.04
The Jackson Laboratory