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Human Disease and Mouse Model Detail
Human Disease Osebold-Remondini Syndrome
OMIM ID: 112910
Human Phenotype Ontology associations
Synonyms Brachydactyly; Brachydactyly, Type A6; BDA6; Brachymesophalangy with Mesomelic Short Limbs and Carpal and Tarsal Osseous Abnormalities
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