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Human Disease and Mouse Model Detail
Human Disease Pontocerebellar Hypoplasia, Type 3; PCH3
OMIM ID: 608027
Synonyms Cerebellar Atrophy with Progressive Microcephaly; CLAM; Pch with Optic Atrophy
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
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
06/05/2013
MGI 5.13 		The Jackson Laboratory