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Terminology chevron_right Concepts chevron_right 725903003

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Component

725903003

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant myoglobinuria (disorder)

Shortest Term

Autosomal dominant myoglobinuria

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Autosomal dominant myoglobinuria (disorder)

SCTID: 725903003, Primitive, Active

725903003|Autosomal dominant myoglobinuria (disorder)|

en Autosomal dominant myoglobinuria
en Autosomal dominant myoglobinuria (disorder)

Expression

725903003 |Autosomal dominant myoglobinuria (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
106102002 |Abnormal urinary product (finding)| + 
240095001 |Lipid storage myopathy (disorder)| + 
48165008 |Myoglobinuria (finding)|
        { 363713009 |Has interpretation (attribute)| = 260373001 |Detected (qualifier value)|,
363714003 |Interprets (attribute)| = 32375007 |Myoglobin measurement, urine (procedure)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3446264015 - Autosomal dominant myoglobinuria (en) View
3446264015	en	Synonym (core metadata concept)	Autosomal dominant myoglobinuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3446263014 - Autosomal dominant myoglobinuria (disorder) (en) View
3446263014	en	Fully specified name (core metadata concept)	Autosomal dominant myoglobinuria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15681311029) - 725903003 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6913225027) - 725903003 -> 52101004 (363713009) View
363713009 \|Has interpretation (attribute)\|	52101004 \|Present (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14972989026) - 725903003 -> 106102002 (116680003) View
116680003 \|Is a (attribute)\|	106102002 \|Abnormal urinary product (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14973004028) - 725903003 -> 260373001 (363713009) View
363713009 \|Has interpretation (attribute)\|	260373001 \|Detected (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6904991022) - 725903003 -> 364687002 (363714003) View
363714003 \|Interprets (attribute)\|	364687002 \|Urine observable (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6904988022) - 725903003 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6904989025) - 725903003 -> 48165008 (116680003) View
116680003 \|Is a (attribute)\|	48165008 \|Myoglobinuria (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6904990023) - 725903003 -> 240095001 (116680003) View
116680003 \|Is a (attribute)\|	240095001 \|Lipid storage myopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913226026) - 725903003 -> 32375007 (363714003) View
363714003 \|Interprets (attribute)\|	32375007 \|Myoglobin measurement, urine (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913227024) - 725903003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913228025) - 725903003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
48165008 View
48165008	Myoglobinuria (finding)	Myoglobinuria	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
106102002 View
106102002	Abnormal urinary product (finding)	Abnormal urinary product	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
240095001 View
240095001	Lipid storage myopathy (disorder)	Lipid storage myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (10fc109d-9454-5b7a-a56c-94a1d5bb5a0e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G73.6	TRUE	ALWAYS G73.6 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|
ExtendedMap object (d3f7114d-a59c-5a36-be8a-f26f929027da) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E75.5	TRUE	ALWAYS E75.5	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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