10623005: Fibrous dysplasia of bone (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Mass of body structure\Mass of musculoskeletal structure\Neoplasm of musculoskeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone

\Musculoskeletal finding\Mass of musculoskeletal structure\Neoplasm of musculoskeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Musculoskeletal finding\Disorder of musculoskeletal system (disorder)\Neoplasm of musculoskeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Musculoskeletal finding\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Musculoskeletal finding\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone

\Disease\Fetal and/or neonatal disorder\Congenital disease\Fibrous dysplasia of bone
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of musculoskeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease (disorder)\Benign neoplasm of bone\Fibrous dysplasia of bone
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Neoplasm of musculoskeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Neoplasm of bone\Benign neoplasm of bone\Fibrous dysplasia of bone

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Fibrous dysplasia of bone	Is a	Disorder of bone (disorder)	false	Inferred relationship	Some
Fibrous dysplasia of bone	Associated morphology	Dysplasia	false	Inferred relationship	Some	1
Fibrous dysplasia of bone	Finding site	Bone structure	false	Inferred relationship	Some	1
Fibrous dysplasia of bone	Finding site	Skeletal system structure	false	Inferred relationship	Some
Fibrous dysplasia of bone	Associated morphology	Dysplasia	false	Inferred relationship	Some	1
Fibrous dysplasia of bone	Finding site	Bone structure	true	Inferred relationship	Some	1
Fibrous dysplasia of bone	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
Fibrous dysplasia of bone	Is a	Benign neoplasm of bone	true	Inferred relationship	Some
Fibrous dysplasia of bone	Is a	Congenital anomaly of skeletal bone	false	Inferred relationship	Some
Fibrous dysplasia of bone	Occurrence	Congenital	true	Inferred relationship	Some	1
Fibrous dysplasia of bone	Associated morphology	Fibrous dysplasia (morphologic abnormality)	true	Inferred relationship	Some	1
Fibrous dysplasia of bone	Is a	Congenital disease	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Dysplasia epiphysealis hemimelica	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Metachondromatosis	Is a	False	Fibrous dysplasia of bone	Inferred relationship	Some
A rare hyaline fibromatosis syndrome with characteristics of papulo-nodular skin lesions (especially around the head and neck), soft tissue masses, gingival hypertrophy, joint contractures and osteolytic bone lesions in variable degrees. Joint contractures may cripple patients and delay normal motor development if occurring in infancy. Severe gingival hyperplasia can interfere with eating and delay dentition. Histopathology analysis of involved tissues reveals cords of spindle-shaped cells embedded in an amorphous, hyaline material.	Is a	False	Fibrous dysplasia of bone	Inferred relationship	Some
Giant cell fibroblastoma of skin (disorder)	Is a	False	Fibrous dysplasia of bone	Inferred relationship	Some
Aggressive infantile fibromatosis	Is a	False	Fibrous dysplasia of bone	Inferred relationship	Some
Juvenile elastofibromatosis (disorder)	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Osteoglophonic dysplasia	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Infantile myofibromatosis	Is a	False	Fibrous dysplasia of bone	Inferred relationship	Some
Polyostotic fibrous dysplasia of bone	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Osteitis fibrosa cystica	Is a	False	Fibrous dysplasia of bone	Inferred relationship	Some
Monostotic fibrous dysplasia	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Fibrous dysplasia of bone with intramuscular myxoma	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
McCune Albright syndrome (disorder)	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Fibrous dysplasia of orbit (disorder)	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
Fibrous dysplasia of jaw	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some
A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive.	Is a	True	Fibrous dysplasia of bone	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
18454016	Fibrous dysplasia of bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
18457011	Osteitis fibrosa	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
579128017	Fibrous dysplasia of bone (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3800192015	Jaffe-Lichtenstein syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1830431000195111	displasia fibrosa dell'osso	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
903331000172118	dysplasie fibreuse des os	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3390961001000117	Knochendysplasie, fibröse	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module