193222002: myopathie congénitale bénigne (trouble)

SNOMED CT Concept\constatation clinique\...

\constatation générale à propos des tissus mous\Disorder of soft tissue\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\constatation à propos d'un muscle\affection musculaire\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\Musculoskeletal finding\maladie du système musculosquelettique (trouble)\...

\Hereditary disorder of musculoskeletal system\Benign congenital myopathy

\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Benign congenital myopathy
\Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\affection musculaire\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Disorder of soft tissue\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\trouble du développement\Developmental hereditary disorder\Benign congenital myopathy
\Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy

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
Benign congenital myopathy	morphologie associée (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some	1
Benign congenital myopathy	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Benign congenital myopathy	est un(e) (attribut)	Developmental hereditary disorder	true	Inferred relationship	Some
Benign congenital myopathy	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	false	Inferred relationship	Some	1
Benign congenital myopathy	est un(e) (attribut)	Congenital disease	false	Inferred relationship	Some
Benign congenital myopathy	survenue (attribut)	congénital	false	Inferred relationship	Some
Benign congenital myopathy	est un(e) (attribut)	Muscular dystrophy	false	Inferred relationship	Some
Benign congenital myopathy	morphologie associée (attribut)	Dystrophy (morphologic abnormality)	false	Inferred relationship	Some	1
Benign congenital myopathy	localisation d'une constatation (attribut)	structure de muscle squelettique	false	Inferred relationship	Some	1
Benign congenital myopathy	est un(e) (attribut)	affection d'un muscle squelettique	false	Inferred relationship	Some
Benign congenital myopathy	est un(e) (attribut)	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Some
Benign congenital myopathy	survenue (attribut)	congénital	false	Inferred relationship	Some	2
Benign congenital myopathy	localisation d'une constatation (attribut)	structure de muscle squelettique	false	Inferred relationship	Some	2
Benign congenital myopathy	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Benign congenital myopathy	localisation d'une constatation (attribut)	structure de muscle squelettique	true	Inferred relationship	Some	1
Benign congenital myopathy	est un(e) (attribut)	Congenital anomaly of skeletal muscle	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign Samaritan congenital myopathy (disorder)	est un(e) (attribut)	True	Benign congenital myopathy	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
297605010	Benign congenital myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
577083019	Benign congenital myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
698851000077119	myopathie congénitale bénigne (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
76371000077117	myopathie congénitale bénigne	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)