FHIR © HL7.org | Server Home | FHIR Server FHIR Server 4.0.1 | FHIR Version n/a User: [n/a]

49347007: Osteosclerosis (disorder)

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

\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)\Disorder of bone development (disorder)\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 (disorder)\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

82200018 Osteosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
787015011 Osteosclerosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2015151000052112 osteoskleros sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core 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
Short stature disorder due to osteosclerosis (disorder)	Due to	True	Osteosclerosis	Inferred relationship	Some	2

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
82200018	Osteosclerosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
787015011	Osteosclerosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2015151000052112	osteoskleros	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)