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Disease Ontology Browser
frontometaphyseal dysplasia (DOID:0111785)
Alliance: disease page
Synonyms: FMD
Alt IDs: MESH:C538064, OMIM:PS305620, ORDO:1826, UMLS_CUI:C0265293
Definition: An otopalatodigital syndrome spectrum disorder characterized by abnormal ossification and skeletal patterning of the axial and appendicular skeleton, facial dysmorphism, urogenital anomalies, and hearing loss.

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
11/12/2024
MGI 6.24 		The Jackson Laboratory