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Human Disease and Mouse Model Detail
Human Disease Catel-Manzke Syndrome
OMIM ID: 302380
Synonyms Hyperphalangy-Clinodactyly of Index Finger with Pierre Robin Syndrome; Index Finger Anomaly with Pierre Robin Syndrome; Micrognathia Digital Syndrome; Palatodigital Syndrome, Catel-Manzke Type; Pierre Robin Syndrome with Hyperphalangy and Clinodactyly
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
08/26/2014
MGI 5.19
The Jackson Laboratory