osteofibrous dysplasia

Summary

osteofibrous dysplasia is a developmental defect during embryogenesis^[1].

Key Facts

• osteofibrous dysplasia's instance of is recorded as developmental defect during embryogenesis^[2].
• osteofibrous dysplasia's instance of is recorded as class of disease^[3].
• osteofibrous dysplasia's subclass of is recorded as primary bone dysplasia^[4].
• osteofibrous dysplasia's subclass of is recorded as ossifying fibroma^[5].
• osteofibrous dysplasia's MeSH descriptor ID is recorded as C563276^[6].
• osteofibrous dysplasia's OMIM ID is recorded as 607278^[7].
• osteofibrous dysplasia's Orphanet ID is recorded as 488265^[8].
• osteofibrous dysplasia's NCI Thesaurus ID is recorded as C53970^[9].
• osteofibrous dysplasia's genetic association is recorded as MET^[10].
• osteofibrous dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_488265^[11].
• osteofibrous dysplasia's UMLS CUI is recorded as C1709353^[12].
• osteofibrous dysplasia's GARD rare disease ID is recorded as 10887^[13].
• osteofibrous dysplasia's Mondo ID is recorded as MONDO_0011806^[14].
• osteofibrous dysplasia's Encyclopedia of China is recorded as 464433^[15].
• osteofibrous dysplasia's UniProt disease ID is recorded as DI-04712^[16].