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Human Disease and Mouse Model Detail
Human Disease Split-Hand/Foot Malformation 3; SHFM3
OMIM ID: 246560
Human Phenotype Ontology associations
Synonyms Chromosome 10q24 Duplication Syndrome; Limb Deficiencies, Distal, with Micrognathia; Shsf3; Split-Hand/Foot Malformation
View all models View ALL (2) mouse models for this human disease.
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 6.07
The Jackson Laboratory