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378007: Morquio syndrome (disorder)

SNOMED CT Concept\constatation clinique\...

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Morquio syndrome
\Disease\Genetic disease\maladie héréditaire\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Morquio syndrome
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Morquio syndrome
\Disease\affection dégénérative\affection dégénérative du système musculosquelettique\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy\Morquio syndrome
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Morquio syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Hereditary disorder of musculoskeletal system\Morquio syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\affection dégénérative du système musculosquelettique\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy\Morquio syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\Degenerative disorder of bone\Osteodystrophy\Congenital osteodystrophy\Morquio syndrome
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Disorder of skeletal system\Disorder of bone (disorder)\maladie métabolique de l'os\Morquio syndrome
\Disease\trouble métabolique\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Morquio syndrome
\Disease\trouble métabolique\Enzymopathy\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Morquio syndrome
\Disease\trouble métabolique\maladie métabolique de l'os\Morquio syndrome
\Disease\Congenital disease\Congenital osteodystrophy\Morquio syndrome
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Mucopolysaccharidosis\Morquio syndrome

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
Morquio syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Morquio syndrome	est un(e) (attribut)	Congenital osteodystrophy	true	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Connective tissue hereditary disorder	false	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Mucopolysaccharidosis	true	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	maladie métabolique de l'os	true	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Osteodystrophy	false	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Congenital anomaly of skeletal bone	false	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Congenital anomaly of cartilage	false	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	affection congénitale du tissu conjonctif	false	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	Connective tissue hereditary disorder	false	Inferred relationship	Some
Morquio syndrome	est un(e) (attribut)	affection dégénérative	false	Inferred relationship	Some
Morquio syndrome	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	true	Inferred relationship	Some	1
Morquio syndrome	localisation d'une constatation (attribut)	structure osseuse	true	Inferred relationship	Some	1
Morquio syndrome	survenue (attribut)	congénital	false	Inferred relationship	Some	2
Morquio syndrome	localisation d'une constatation (attribut)	structure osseuse	false	Inferred relationship	Some
Morquio syndrome	localisation d'une constatation (attribut)	Cartilaginous tissue structure	false	Inferred relationship	Some
Morquio syndrome	localisation d'une constatation (attribut)	Skeletal system structure	false	Inferred relationship	Some
Morquio syndrome	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Mucopolysaccharidosis, MPS-IV-A	est un(e) (attribut)	True	Morquio syndrome	Inferred relationship	Some
Mucopolysaccharidosis, MPS-IV-B	est un(e) (attribut)	True	Morquio syndrome	Inferred relationship	Some
syndrome de François	est un(e) (attribut)	False	Morquio syndrome	Inferred relationship	Some

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)

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Id	Description	Lang	Type	Status	Case?	Module
170353012	Morquio syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
177745017	Chondro-osteodystrophy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
177746016	Morquio-Suarez syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
177747013	Morquio-Ullrich disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
177748015	Osteochondrodystrophia deformans	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
177749011	Atypical chondrodystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178139018	Morquio disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
178195010	Familial osteochondrodystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178196011	Brailsford-Morquio syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
178340010	Hereditary enchondral dysostosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178342019	Chondrodystrophia tarda	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178343012	Familial osseous dystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
178344018	Keratan sulfaturia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
199284013	Mucopolysaccharidosis, MPS-IV	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
486813017	Morquio-Brailsford disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
486814011	Osteochondrodystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
486815012	Mucopolysaccharidosis type IV	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
486816013	Keratan sulphaturia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
67531000077119	mucopolysaccharidose type IV	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
689751000077117	mucopolysaccharidose type IV (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
769710010	Morquio syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core