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Diseases

Osteitis Fibrosa Disseminata

osteitis fibrosa disseminata

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Osteitis Fibrosa Disseminata
Standard Disease Name
osteitis fibrosa disseminata
MeSH Tree
No data
ICD-10
No data

Identifiers

DO ID
No data
MeSH ID
D005357
OMIM ID
No data
UMLS ID
C0016063
HPO ID
No data

Description and Extensions

Description
MSH2017_2016_08_12: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).|HPO2016_07_04:Tumor-like growths that consist of replacement of the medullary bone with fibrous tissue, causing the expansion and weakening of the areas of bone involved. Especially when involving the skull or facial bones, the lesions can cause externally visible deformities. The skull is often, but not necessarily, affected, and any other bone or bones may be involved. Fibrous dysplasia can either effect isolated bones (Monostotic fibrous dysplasia) or also generalized all bones of the body (Polyostotic fibrous dysplasia). [HPO:sdoelken]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
06
RUNX2
RUNX family transcription factor 2
RUNX family transcription factor 2