1234828008: Osteofibrous dysplasia (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of limb structure\Disorder of extremity\Disorder of lower extremity\Disorder of free lower limb\Disorder of lower leg\Osteofibrous dysplasia
\Finding of limb structure\Finding of lower limb\Finding of bone of lower limb\Osteofibrous dysplasia
\Finding of limb structure\Finding of lower limb\Disorder of lower extremity\Disorder of free lower limb\Disorder of lower leg\Osteofibrous dysplasia

\Musculoskeletal finding\Bone finding\Finding of bone of lower limb\Osteofibrous dysplasia
\Musculoskeletal finding\Bone finding\Disorder of bone\Degenerative disorder of bone\Osteofibrous dysplasia
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteofibrous dysplasia
\Musculoskeletal finding\Disorder of musculoskeletal system\Degenerative disorder of musculoskeletal system\Degenerative disorder of bone\Osteofibrous dysplasia
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteofibrous dysplasia
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Degenerative disorder of bone\Osteofibrous dysplasia
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteofibrous dysplasia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteofibrous dysplasia
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Osteofibrous dysplasia
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Osteofibrous dysplasia
\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system\Degenerative disorder of bone\Osteofibrous dysplasia
\Disease\Degenerative disorder\Calcinosis\Heterotopic ossification\Osteofibrous dysplasia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteofibrous dysplasia
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteofibrous dysplasia
\Disease\Disorder of body system\Disorder of musculoskeletal system\Degenerative disorder of musculoskeletal system\Degenerative disorder of bone\Osteofibrous dysplasia
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Osteofibrous dysplasia
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Degenerative disorder of bone\Osteofibrous dysplasia
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteofibrous dysplasia
\Disease\Disorder of extremity\Disorder of lower extremity\Disorder of free lower limb\Disorder of lower leg\Osteofibrous dysplasia
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteofibrous dysplasia
\Disease\Developmental disorder\Developmental hereditary disorder\Osteofibrous dysplasia
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Osteofibrous dysplasia

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

5084156018 Osteofibrous dysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5084157010 Osteofibrous dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Osteofibrous dysplasia	Is a	Congenital skeletal dysplasia	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Disorder of lower leg	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Heterotopic ossification	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Degenerative disorder of bone	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Is a	Finding of bone of lower limb	true	Inferred relationship	Existential restriction modifier
Osteofibrous dysplasia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Osteofibrous dysplasia	Finding site	Skeletal system structure	true	Inferred relationship	Existential restriction modifier	2
Osteofibrous dysplasia	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	2
Osteofibrous dysplasia	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Osteofibrous dysplasia	Finding site	Bone structure of lower leg	true	Inferred relationship	Existential restriction modifier	1
Osteofibrous dysplasia	Associated morphology	Fibro-osseous pseudotumor	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
5084156018	Osteofibrous dysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
5084157010	Osteofibrous dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module