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Human Disease and Mouse Model Detail
Human Disease

Term: Chromosome Xp22 Deletion Syndrome
OMIM ID: 300830

Synonyms Autism, Susceptibility to, X-Linked 4; AUTSX4
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
Citing These Resources
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory