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Human Disease and Mouse Model Detail
Human Disease Chromosome 19q13.11 Deletion Syndrome, Distal
OMIM ID: 613026
Human Phenotype Ontology associations
Synonyms Chromosome Deletion Syndrome
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
11/29/2016
MGI 6.06
The Jackson Laboratory