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Human Disease and Mouse Model Detail
Human Disease

Term: Russell-Silver Syndrome, X-Linked
OMIM ID: 312780

Synonyms Partington Syndrome; Russell-Silver-Like Syndrome with Skin Pigmentation
Associated Genes
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
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last database update
04/03/2013
MGI 5.12
The Jackson Laboratory