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Human Disease and Mouse Model Detail
Human Disease Shprintzen Omphalocele Syndrome
OMIM ID: 182210
Human Phenotype Ontology associations
Synonyms Omphalocele with Hypoplasia of Pharynx and Larynx, Learning Disability, Dysmorphic Facies, and Scoliosis; Pharynx and Larynx Hypoplasia with Omphalocele
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