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Descriptor English: Fibrous Dysplasia of Bone
Descriptor Spanish: Displasia Fibrosa Ósea
Descriptor displasia fibrosa ósea
Entry term(s) displasia fibrosa del hueso
displasia ósea fibrocartilaginosa
displasias óseas fibrocartilaginosas
osteítis fibrosa diseminada
Scope note: Enfermedad ósea caracterizada por adelgazamiento de la cortical a causa de tejido fibroso que contiene espículas óseas, lo que produce dolor, incapacidad y deformidad de implantación gradual. Puede que se afecte un solo hueso (DISPLASIA FIBROSA MONOSTÓTICA) o varios huesos (DISPLASIA FIBROSA POLIOSTÓTICA)
Descriptor Portuguese: Displasia Fibrosa Óssea
Descriptor French: Dysplasie fibreuse des os
Entry term(s): Bone Fibrocartilaginous Dysplasia
Bone Fibrocartilaginous Dysplasias
Bone Fibrocystic Dysplasia
Bone Fibrocystic Dysplasias
Bone Fibrous Dysplasia
Bone Fibrous Dysplasias
Fibrocartilaginous Dysplasia of Bone
Fibrocystic Dysplasia of Bone
Jaffe Lichtenstein Disease
Jaffe-Lichtenstein Disease
Osteitis Fibrosa Disseminata
Tree number(s): C05.116.099.708.375
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D005357
Scope note: A disease of bone marked by thinning of the cortex by fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC).
Annotation: PERIAPICAL FIBROUS DYSPLASIA see CEMENTOMA is also available
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 67; ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE were see under OSTEITIS FIBROSA 1963-66
Online Note: use FIBROUS DYSPLASIA OF BONE to search FIBROUS DYSPLASIA 1966 (as Prov); search ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE under OSTEITIS FIBROSA CYSTICA 1966
History Note: 67; was FIBROUS DYSPLASIA 1963-66 (Prov); ALBRIGHT'S DISEASE & JAFFE-LICHTENSTEIN DISEASE were see under OSTEITIS FIBROSA 1963-66
DeCS ID: 5493
Unique ID: D005357
NLM Classification: WE 250
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1967/01/01
Date of Entry: 1999/01/01
Revision Date: 2018/03/08
Fibrous Dysplasia of Bone - Preferred
Concept UI M0008455
Scope note A disease of bone marked by thinning of the cortex by fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC).
Preferred term Fibrous Dysplasia of Bone
Entry term(s) Bone Fibrous Dysplasia
Bone Fibrous Dysplasias
Jaffe Lichtenstein Disease
Jaffe-Lichtenstein Disease
Osteitis Fibrosa Disseminata
Fibrocystic Dysplasia of Bone - Related but not broader or narrower
Concept UI M000639769
Preferred term Fibrocystic Dysplasia of Bone
Entry term(s) Bone Fibrocystic Dysplasia
Bone Fibrocystic Dysplasias
Fibrocartilaginous Dysplasia of Bone - Narrower
Concept UI M000639771
Preferred term Fibrocartilaginous Dysplasia of Bone
Entry term(s) Bone Fibrocartilaginous Dysplasia
Bone Fibrocartilaginous Dysplasias



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