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Disease Ontology Browser
otopalatodigital syndrome spectrum disorder (DOID:0111782)
Alliance: disease page
Synonyms: fronto-otopalatodigital osteodysplasia; OPD spectrum disorder; OPSD
Alt IDs: ORDO:364541
Definition: A bone development disease characterized by typical facial anomalies and a generalized bone dysplasia with osteodysplastic changes with skeletal dysplasia developing as varying combinations and degrees of undertubulation of the long bones, cortical irregularity and campomelia. Most but not all subtypes are associated with mutations in FLNA on chromosome Xq28.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory