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Disease Ontology Browser
Ehlers-Danlos syndrome periodontal type 2 (DOID:0080987)
Alliance: disease page
Alt IDs: OMIM:617174, ORDO:75392
Definition: An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the C1S gene on chromosome 12p13.


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
11/12/2024
MGI 6.24
The Jackson Laboratory