About   Help   FAQ
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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 5.20
The Jackson Laboratory