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Disease Ontology Browser
obsolete SC phocomelia syndrome (DOID:0050536)
Alliance: disease page
Definition: A syndrome that is characterized by severe prenatal growth retardation resulting in malformation of the bones in the skull, face and limbs, has_material_basis_in the mutation in the ESCO2 gene.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
07/13/2021
MGI 6.17
The Jackson Laboratory