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Human Disease and Mouse Model Detail
Human Disease Megarbane-Jalkh Syndrome
OMIM ID: 612785
Synonyms Developmental Delay, Dysmorphic Features, Neonatal Spontaneous Fractures, Wrinkled Skin, and Hepatic Failure
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 6.03
The Jackson Laboratory