205497004: Osteogenesis imperfecta type IV (disorder)

SNOMED CT Concept\constatation clinique\...

\constatation fonctionnelle\Abnormal bone formation\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form

\Musculoskeletal finding\constatation à propos de l'os\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Musculoskeletal finding\constatation à propos de l'os\Abnormal bone formation\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form

\Disease\Genetic disease\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\trouble du développement\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Osteogenesis imperfecta\Osteogenesis imperfecta with normal sclerae, dominant form

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Osteogenesis imperfecta with normal sclerae, dominant form	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	2
Osteogenesis imperfecta with normal sclerae, dominant form	interprète (attribut)	Bone formation, function (observable entity)	true	Inferred relationship	Some	2
Osteogenesis imperfecta with normal sclerae, dominant form	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	est un(e) (attribut)	Osteogenesis imperfecta	true	Inferred relationship	Some
Osteogenesis imperfecta with normal sclerae, dominant form	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	localisation d'une constatation (attribut)	Skeletal system structure	false	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	survenue (attribut)	congénital	false	Inferred relationship	Some
Osteogenesis imperfecta with normal sclerae, dominant form	localisation d'une constatation (attribut)	Connective tissue	false	Inferred relationship	Some
Osteogenesis imperfecta with normal sclerae, dominant form	localisation d'une constatation (attribut)	structure osseuse	true	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	morphologie associée (attribut)	dysplasie	true	Inferred relationship	Some	1
Osteogenesis imperfecta with normal sclerae, dominant form	localisation d'une constatation (attribut)	Connective tissue structure	false	Inferred relationship	Some
Osteogenesis imperfecta with normal sclerae, dominant form	survenue (attribut)	congénital	false	Inferred relationship	Some	2
Osteogenesis imperfecta with normal sclerae, dominant form	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	2
Osteogenesis imperfecta with normal sclerae, dominant form	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Osteogenesis imperfecta, type IV B	est un(e) (attribut)	True	Osteogenesis imperfecta with normal sclerae, dominant form	Inferred relationship	Some
Osteogenesis imperfecta, type IV A	est un(e) (attribut)	True	Osteogenesis imperfecta with normal sclerae, dominant form	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
315124015	Osteogenesis imperfecta type IV	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
315125019	Osteogenesis imperfecta, type IV	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
315126018	Osteogenesis imperfecta with normal sclerae, dominant form	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
527851000241118	ostéogenèse imparfaite type 4 (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
590872019	Osteogenesis imperfecta type IV (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
909401000172119	OI type 4 - ostéogenèse imparfaite type 4	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
980201000172110	ostéogenèse imparfaite type 4	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)