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Disease Ontology Browser
hypochondroplasia (DOID:0080041)
Alliance: disease page
Alt IDs: OMIM:146000, ICD10CM:Q77.4, MESH:C562937, ORDO:429, UMLS_CUI:C0410529
Definition: An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism.


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
02/18/2020
MGI 6.14
The Jackson Laboratory