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Human Disease and Mouse Model Detail
Human Disease Granddad Syndrome
OMIM ID: 138920
Human Phenotype Ontology associations
Synonyms Growth Retardation, Aged Facies, Normal Development, Decreased Subcutaneous Fat, Autosomal Dominant Inheritance
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