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Human Disease and Mouse Model Detail
Human Disease Lambert Syndrome
OMIM ID: 245550
Human Phenotype Ontology associations
Synonyms Branchial Dysplasia, Clubfoot, Inguinal Hernia, and Biliary Atresia
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
Citing These Resources
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last database update
MGI 6.07
The Jackson Laboratory