193225000: Hereditary progressive muscular dystrophy (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy

\Muscle finding\Disorder of skeletal AND/OR smooth muscle\...

\Degenerative disorder of muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy

\Disorder of skeletal muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy

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

\Hereditary disorder of musculoskeletal system\Hereditary progressive muscular dystrophy

\Degenerative disorder of musculoskeletal system\Muscular dystrophy\Hereditary progressive muscular dystrophy

\Chronic disease of musculoskeletal system\Muscular dystrophy\Hereditary progressive muscular dystrophy

\Disorder of skeletal muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy

\Disease\Genetic disease\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Hereditary progressive muscular dystrophy
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Hereditary progressive muscular dystrophy
\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Degenerative disorder\Degenerative disorder of muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Hereditary progressive muscular dystrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Hereditary progressive muscular dystrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Degenerative disorder of musculoskeletal system\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Chronic disease of musculoskeletal system\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Disorder of skeletal AND/OR smooth muscle\Degenerative disorder of muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Disorder of skeletal AND/OR smooth muscle\Disorder of skeletal muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Chronic disease\Chronic disease of musculoskeletal system\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Muscular dystrophy\Hereditary progressive muscular dystrophy
\Disease\Developmental disorder\Developmental hereditary disorder\Hereditary progressive muscular dystrophy
\Disease\Developmental disorder\Muscular dystrophy\Hereditary progressive muscular dystrophy

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

297608012 Hereditary progressive muscular dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

577087018 Hereditary progressive muscular dystrophy (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
Hereditary progressive muscular dystrophy	Is a	Muscular dystrophy	true	Inferred relationship	Existential restriction modifier
Hereditary progressive muscular dystrophy	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier	1
Hereditary progressive muscular dystrophy	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier	1
Hereditary progressive muscular dystrophy	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier	1
Hereditary progressive muscular dystrophy	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier	1
Hereditary progressive muscular dystrophy	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Hereditary progressive muscular dystrophy	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier
Hereditary progressive muscular dystrophy	Clinical course	Progressive	true	Inferred relationship	Existential restriction modifier	2
Hereditary progressive muscular dystrophy	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Bethlem myopathy	Is a	False	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Adult-onset distal myopathy due to valosin containing protein mutation	Is a	False	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Distal muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Muscular dystrophy with predominantly proximal limb girdle distribution	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Congenital hereditary muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
X-linked scapuloperoneal muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Severe childhood autosomal recessive muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Autosomal dominant Emery-Dreifuss muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Steinert myotonic dystrophy syndrome	Is a	False	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Autosomal recessive Emery-Dreifuss muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
X-linked Emery-Dreifuss muscular dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
X-linked myopathy with postural muscle atrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Myotonic dystrophy	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome	Is a	True	Hereditary progressive muscular dystrophy	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
297608012	Hereditary progressive muscular dystrophy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
577087018	Hereditary progressive muscular dystrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module