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Human Disease and Mouse Model Detail
Human Disease GOMBO Syndrome
OMIM ID: 233270
Synonyms Growth Retardation, Ocular Abnormalities, Microcephaly, Brachydactyly, and Oligophrenia
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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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory