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SNOMED CT
Last uploaded:
January 16, 2025
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Id | http://purl.bioontology.org/ontology/SNOMEDCT/55133004
http://purl.bioontology.org/ontology/SNOMEDCT/55133004
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Preferred Name | Multi-core congenital myopathy |
Synonyms |
Multi-core congenital myopathy (disorder)
Multiminicore disease
Multi-core disease
Minicore disease
Multicore disease
Multi-minicore disease
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
altLabel |
Multi-core congenital myopathy (disorder)
Multiminicore disease
Multi-core disease
Minicore disease
Multicore disease
Multi-minicore disease
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prefLabel | Multi-core congenital myopathy
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Type ID |
900000000000003001
900000000000013009
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CASE SIGNIFICANCE ID | 900000000000448009
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notation | 55133004
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Effective time | 20020131
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Active | 1
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Has finding site | |
Has pathological process | |
subClassOf | |
Semantic type UMLS property | |
type | |
Subset member | 447562003~MAPRULE~TRUE
6011000124106~MAPTARGET~H49.889
447562003~MAPTARGET~G71.2
6011000124106~MAPTARGET~Q74.3
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
900000000000497000~MAPTARGET~X7092
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPRULE~IFA 1259119003 | Antenatal multi-minicore disease with arthrogryposis multiplex congenita |
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
447562003~MAPADVICE~ALWAYS G71.2
6011000124106~MAPADVICE~IF CONGENITAL MULTI-MINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA CHOOSE H49.889 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF ANTENATAL MULTI-MINICORE DISEASE WITH ARTHROGRYPOSIS MULTIPLEX CONGENITA CHOOSE G71.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~ALWAYS G71.29
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPADVICE~IF CONGENITAL MULTI-MINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA CHOOSE G71.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF ANTENATAL MULTI-MINICORE DISEASE WITH ARTHROGRYPOSIS MULTIPLEX CONGENITA CHOOSE Q74.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~MAPRULE~IFA 1259560001 | Congenital multi-minicore disease with external ophthalmoplegia |
6011000124106~CORRELATIONID~447561005
6011000124106~MAPTARGET~G71.2
6011000124106~MAPRULE~TRUE
6011000124106~MAPTARGET~G71.29
6011000124106~MAPPRIORITY~3
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
6011000124106~MAPADVICE~ALWAYS G71.2
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DEFINITION STATUS ID | 900000000000074008
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tui | T047
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CTV3ID | X7092
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Occurs in | |
cui | C0270962
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Has associated morphology |
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