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49347007: Osteosclerosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Bone finding\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteosclerosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteosclerosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteosclerosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Osteosclerosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone\Disorder of bone development\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Osteosclerosis
\Disease\Developmental disorder\Disorder of bone development\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Developmental disorder\Developmental hereditary disorder\Osteosclerosis
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

82200018 Osteosclerosis en Synonym Active Entire term case insensitive SNOMED CT core module

787015011 Osteosclerosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Osteosclerosis	Is a	Disorder of bone	false	Inferred relationship	Existential restriction modifier
Osteosclerosis	Associated morphology	Bony sclerosis	false	Inferred relationship	Existential restriction modifier
Osteosclerosis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier
Osteosclerosis	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier
Osteosclerosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Osteosclerosis	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Osteosclerosis	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Osteosclerosis	Associated morphology	Bony sclerosis	true	Inferred relationship	Existential restriction modifier	1
Osteosclerosis	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier
Osteosclerosis	Is a	Chronic disease of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Osteosclerosis	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier	1
Osteosclerosis	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier	2
Osteosclerosis	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Osteosclerosis - Stanescu type	Is a	False	Osteosclerosis	Inferred relationship	Existential restriction modifier
Axial osteosclerosis	Is a	True	Osteosclerosis	Inferred relationship	Existential restriction modifier
Piriform sclerosis of ilium	Is a	False	Osteosclerosis	Inferred relationship	Existential restriction modifier
Chronic symmetric plasma cell osteomyelitis	Is a	False	Osteosclerosis	Inferred relationship	Existential restriction modifier
Osteosclerosis, developmental delay, craniosynostosis syndrome	Is a	False	Osteosclerosis	Inferred relationship	Existential restriction modifier
Dentin dysplasia with sclerotic bone syndrome	Is a	True	Osteosclerosis	Inferred relationship	Existential restriction modifier
Melorheostosis	Is a	False	Osteosclerosis	Inferred relationship	Existential restriction modifier
Short stature disorder due to osteosclerosis	Due to	True	Osteosclerosis	Inferred relationship	Existential restriction modifier	2
Hyperostosis cranialis interna	Is a	True	Osteosclerosis	Inferred relationship	Existential restriction modifier
Osteosclerotic metaphyseal dysplasia	Is a	True	Osteosclerosis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
82200018	Osteosclerosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
787015011	Osteosclerosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module