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193222002: Benign congenital myopathy (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\Muscle finding\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy

\Musculoskeletal finding\Disorder of musculoskeletal system\...

\Hereditary disorder of musculoskeletal system\Benign congenital myopathy

\Disorder of skeletal muscle\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\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Benign congenital myopathy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Benign congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\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\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Benign congenital myopathy
\Disease\Developmental disorder\Developmental hereditary disorder\Benign congenital myopathy
\Disease\Developmental disorder\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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

297605010 Benign congenital myopathy en Synonym Active Entire term case insensitive SNOMED CT core module

577083019 Benign congenital myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Benign congenital myopathy	Is a	Muscular dystrophy	false	Inferred relationship	Existential restriction modifier
Benign congenital myopathy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Is a	Congenital disease	false	Inferred relationship	Existential restriction modifier
Benign congenital myopathy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Benign congenital myopathy	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Is a	Disorder of skeletal muscle	false	Inferred relationship	Existential restriction modifier
Benign congenital myopathy	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Benign congenital myopathy	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Benign congenital myopathy	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	2
Benign congenital myopathy	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Is a	Congenital anomaly of skeletal muscle	true	Inferred relationship	Existential restriction modifier
Benign congenital myopathy	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Benign congenital myopathy	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Benign Samaritan congenital myopathy	Is a	True	Benign congenital myopathy	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
297605010	Benign congenital myopathy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
577083019	Benign congenital myopathy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module