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Human Disease and Mouse Model Detail
Human Disease Myopia 17, Autosomal Dominant; MYP17
OMIM ID: 608367
Human Phenotype Ontology associations
Synonyms Myopia; Myopia 4, Formerly; MYP4, FORMERLY
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
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last database update
MGI 6.07
The Jackson Laboratory