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Human Disease and Mouse Model Detail
Human Disease

Term: Mesomelia-Synostoses Syndrome
OMIM ID: 600383

Synonyms Chromosome 8q13 Deletion Syndrome; Mesomelic Dysplasia, Syndromic; Mesomelic Dysplasia with Acral Synostoses, Verloes-David-Pfeiffer Type
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