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Disease Ontology Browser
craniometaphyseal dysplasia (DOID:0080033)
Alliance: disease page
Alt IDs: OMIM:122860, OMIM:123000, OMIM:218400, OMIM:614099, OMIM:614378, ORDO:1522
Definition: An osteosclerosis that has_material_basis_in mutations in the ANKH gene which results_in progressive thickening located_in skull and abnormally shaped ends of long bones in the limbs.

Disease References using Mouse Models (3)

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
06/11/2019
MGI 6.14
The Jackson Laboratory