32985001: Greig cephalopolysyndactyly syndrome (disorder)

SNOMED CT Concept\constatation clinique\...

\Musculoskeletal finding\constatation à propos de l'os\Disorder of bone (disorder)\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\syndrome de céphalopolysyndactylie de Greig (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\syndrome de céphalopolysyndactylie de Greig (trouble)
\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\syndrome de céphalopolysyndactylie de Greig (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\syndrome de céphalopolysyndactylie de Greig (trouble)
\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\syndrome de céphalopolysyndactylie de Greig (trouble)

\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Skeletal dysplasia\syndrome de céphalopolysyndactylie de Greig (trouble)
\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\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\trouble du développement\Disorder of bone development (disorder)\Congenital anomaly of skeletal bone\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Skeletal dysplasia\syndrome de céphalopolysyndactylie de Greig (trouble)
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\syndrome de céphalopolysyndactylie de Greig (trouble)

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
syndrome de céphalopolysyndactylie de Greig (trouble)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	survenue (attribut)	congénital	true	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	est un(e) (attribut)	Congenital anomaly of skeletal bone	true	Inferred relationship	Some
syndrome de céphalopolysyndactylie de Greig (trouble)	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	est un(e) (attribut)	Skeletal dysplasia	true	Inferred relationship	Some
syndrome de céphalopolysyndactylie de Greig (trouble)	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	survenue (attribut)	congénital	false	Inferred relationship	Some	2
syndrome de céphalopolysyndactylie de Greig (trouble)	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some	2
syndrome de céphalopolysyndactylie de Greig (trouble)	morphologie associée (attribut)	Congenital dysplasia	false	Inferred relationship	Some	2
syndrome de céphalopolysyndactylie de Greig (trouble)	localisation d'une constatation (attribut)	Skeletal system structure	false	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	survenue (attribut)	congénital	false	Inferred relationship	Some
syndrome de céphalopolysyndactylie de Greig (trouble)	localisation d'une constatation (attribut)	structure osseuse	true	Inferred relationship	Some	1
syndrome de céphalopolysyndactylie de Greig (trouble)	morphologie associée (attribut)	dysplasie	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
418121000241118	syndrome de céphalopolysyndactylie de Greig (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
55063010	Greig cephalopolysyndactyly syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
764332017	Greig cephalopolysyndactyly syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
880811000172117	syndrome de céphalopolysyndactylie de Greig	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
903601000172115	GCPS - Greig cephalopolysyndactyly syndrome	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)