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Human Disease and Mouse Model Detail
Human Disease Microphthalmia, Syndromic 1; MCOPS1
OMIM ID: 309800
Synonyms Lenz Dysplasia; Lenz Microphthalmia Syndrome; Maa, Formerly; Microphthalmia, Syndromic
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 5.17
The Jackson Laboratory