JSON

fibrous dysplasia

^ http://purl.obolibrary.org/obo/MONDO_0000845

A genetic, non-inheritable disorder caused by osteoblastic differentiation defects that result in the replacement of bone marrow and trabecular bone by fibrous stroma and immature bone. It usually affects a single bone and less frequently multiple bones. Skull, femur, tibia, and humerus are the most frequently affected bones. It manifests with pain, deformities, and fractures. [ NCIT:C34609 ]

Term info

database cross reference
  • NCIT:C34609 (MONDO:equivalentTo)
  • MedDRA:10016664 (Orphanet:249/e)
  • SCTID:254145001 (MONDO:equivalentTo)
  • MESH:D005357 (Orphanet:249/e)
  • Orphanet:249 (MONDO:equivalentTo)
  • SCTID:10623005 (MONDO:equivalentTo)
  • ICD9:733.29 (MONDO:relatedTo)
  • GARD:0006444 (MONDO:equivalentTo)
  • DOID:0080031 (MONDO:equivalentTo)
Subsets

ordo_malformation_syndrome

closeMatch

http://identifiers.org/meddra/10016664

definition

A genetic, non-inheritable disorder caused by osteoblastic differentiation defects that result in the replacement of bone marrow and trabecular bone by fibrous stroma and immature bone. It usually affects a single bone and less frequently multiple bones. Skull, femur, tibia, and humerus are the most frequently affected bones. It manifests with pain, deformities, and fractures.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_249, http://purl.obolibrary.org/obo/DOID_0080031, http://identifiers.org/snomedct/254145001, http://identifiers.org/mesh/D005357, http://identifiers.org/snomedct/10623005, http://purl.obolibrary.org/obo/NCIT_C34609

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019708

has exact synonym

fibrous dysplasia of bone

id

MONDO:0000845