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

Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

787015011 Osteosclerosis (disorder) en Fully specified name Active Case insensitive SNOMED CT core
82200018 Osteosclerosis en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

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

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

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start

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