75491005: Amyotrophia congenita (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\...

\Hypoplasia of muscle\Amyotrophia congenita

\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita

\Muscle atrophy\Amyotrophia congenita

\Muscle finding (finding)\Disorder of muscle\...

\Degenerative disorder of muscle (disorder)\Muscle atrophy\Amyotrophia congenita

\Disorder of skeletal muscle\Hypoplasia of muscle\Amyotrophia congenita
\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disorder of skeletal muscle\Muscle atrophy\Amyotrophia congenita

\Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\...

\Degenerative disorder of musculoskeletal system (disorder)\Muscle atrophy\Amyotrophia congenita

\Disorder of skeletal muscle\Hypoplasia of muscle\Amyotrophia congenita
\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disorder of skeletal muscle\Muscle atrophy\Amyotrophia congenita

\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disease\Degenerative disorder\Degenerative disorder of musculoskeletal system (disorder)\Muscle atrophy\Amyotrophia congenita
\Disease\Degenerative disorder\Degenerative disorder of muscle (disorder)\Muscle atrophy\Amyotrophia congenita
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Degenerative disorder of musculoskeletal system (disorder)\Muscle atrophy\Amyotrophia congenita
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Hypoplasia of muscle\Amyotrophia congenita
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Muscle atrophy\Amyotrophia congenita
\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disease\Disorder of muscle\Degenerative disorder of muscle (disorder)\Muscle atrophy\Amyotrophia congenita
\Disease\Disorder of muscle\Disorder of skeletal muscle\Hypoplasia of muscle\Amyotrophia congenita
\Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disease\Disorder of muscle\Disorder of skeletal muscle\Muscle atrophy\Amyotrophia congenita
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Hypoplasia of muscle\Amyotrophia congenita
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita
\Disease\Disorder of soft tissue\Disorder of skeletal muscle\Muscle atrophy\Amyotrophia congenita
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Amyotrophia congenita

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
Amyotrophia congenita	Is a	Muscle atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyotrophia congenita	Is a	Congenital anomaly of skeletal muscle (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyotrophia congenita	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Associated morphology	Congenital hypoplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Associated morphology	Congenital atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyotrophia congenita	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Is a	Hypoplasia of muscle	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Finding site	Skeletal muscle structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Amyotrophia congenita	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Amyotrophia congenita	Finding site	Skeletal muscle structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Amyotrophia congenita	Associated morphology	Atrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Amyotrophia congenita	Associated morphology	Hypoplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Amyotrophia congenita	Associated morphology	Atrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Amyotrophia congenita	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Amyotrophia congenita	Associated morphology	Hypoplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
125385010	Amyotrophia congenita	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
816106017	Amyotrophia congenita (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
125385010	Amyotrophia congenita	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
125385010	Amyotrophia congenita	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
816106017	Amyotrophia congenita (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
816106017	Amyotrophia congenita (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4636731000241117	amyotrophie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4636731000241117	amyotrophie congénitale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module