About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Megarbane-Jalkh Syndrome
OMIM ID: 612785

Synonyms Developmental Delay, Dysmorphic Features, Neonatal Spontaneous Fractures, Wrinkled Skin, and Hepatic Failure
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
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory