49347007: Osteosclerosis (disorder)

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

\Finding by site\Disorder by body site (disorder)\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Finding by site\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Finding by site\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteosclerosis
\Finding by site\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteosclerosis
\Finding by site\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteosclerosis
\Finding by site\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteosclerosis
\Finding by site\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Finding by site\Musculoskeletal finding\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteosclerosis
\Finding by site\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteosclerosis
\Finding by site\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 by body site (disorder)\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Osteosclerosis
\Disease\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Osteosclerosis
\Disease\Disorder by body site (disorder)\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteosclerosis
\Disease\Disorder by body site (disorder)\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 (disorder)\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 (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module	Reference Sets
82200018	Osteosclerosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Preferred (foundation metadata concept)
787015011	Osteosclerosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core	GB English: Preferred (foundation metadata concept)
2015151000052112	osteoskleros	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)	Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Osteosclerosis	Is a	Disorder of bone (disorder)	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
Osteosclerosis	Occurrence	Congenital	true	Inferred relationship	Some	1
Osteosclerosis	Pathological process (attribute)	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 (qualifier value)	true	Inferred relationship	Some	2
Osteosclerosis	Is a	Developmental hereditary disorder	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Osteosclerosis - Stanescu type	Is a	False	Osteosclerosis	Inferred relationship	Some
Axial osteosclerosis (disorder)	Is a	True	Osteosclerosis	Inferred relationship	Some
Piriform sclerosis of ilium (disorder)	Is a	False	Osteosclerosis	Inferred relationship	Some
Chronic symmetric plasma cell osteomyelitis (disorder)	Is a	False	Osteosclerosis	Inferred relationship	Some
Osteosclerosis, developmental delay, craniosynostosis syndrome (disorder)	Is a	False	Osteosclerosis	Inferred relationship	Some
Dentin dysplasia with sclerotic bone syndrome	Is a	True	Osteosclerosis	Inferred relationship	Some
Melorheostosis	Is a	False	Osteosclerosis	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set

GB English

US English

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