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Human Disease and Mouse Model Detail
Human Disease Mesomelia-Synostoses Syndrome
OMIM ID: 600383
Human Phenotype Ontology associations
Synonyms Chromosome 8q13 Deletion Syndrome; Mesomelic Dysplasia with Acral Synostoses, Verloes-David-Pfeiffer Type; Mesomelic Dysplasia, Syndromic
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
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last database update
MGI 6.07
The Jackson Laboratory