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Disease Ontology Browser
metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome (DOID:0111513)
Alliance: disease page
Synonyms: metaphyseal dysplasia maxillary hypoplasia brachydactyly; metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly
Alt IDs: OMIM:156510, ORDO:2504
Definition: An osteochondrodysplasia characterized by metaphyseal flaring of long bones, enlargement of the medial halves of the clavicles, maxillary hypoplasia, variable brachydactyly, and dystrophic teeth that has_material_basis_in heterozygous duplication of RUNX2 on chromosome 6p21.1.


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
02/11/2020
MGI 6.14
The Jackson Laboratory