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Terminology chevron_right Concepts chevron_right 773644000

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Component

773644000

The component that hold information about this concept.

Fully Specified Name (FSN)

Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)

Shortest Term

Progeroid and marfanoid aspect, lipodystrophy syndrome

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

Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)

SCTID: 773644000, Primitive, Active

773644000|Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)|

en Progeroid and marfanoid aspect, lipodystrophy syndrome
en Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)

Expression

773644000 |Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)|
 <<< 363070008 |Developmental hereditary disorder (disorder)| + 
65094009 |Multiple malformation syndrome with facial defects as major feature (disorder)| + 
56759000 |Congenital anomaly of subcutaneous tissue (disorder)| + 
399959003 |Premature aging syndrome (disorder)| + 
19346006 |Marfan's syndrome (disorder)| + 
724841000 |Genetic lipodystrophy (disorder)| + 
363039000 |Congenital connective tissue disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 67769002 |Structure of subcutaneous fatty tissue (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 89545001 |Face structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3725349010 - Progeroid and marfanoid aspect, lipodystrophy syndrome (en) View
3725349010	en	Synonym (core metadata concept)	Progeroid and marfanoid aspect, lipodystrophy syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3725348019 - Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder) (en) View
3725348019	en	Fully specified name (core metadata concept)	Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13070002026) - 773644000 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11471128022) - 773644000 -> 363039000 (116680003) View
116680003 \|Is a (attribute)\|	363039000 \|Congenital connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624933023) - 773644000 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624934028) - 773644000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624935027) - 773644000 -> 65094009 (116680003) View
116680003 \|Is a (attribute)\|	65094009 \|Multiple malformation syndrome with facial defects as major feature (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624936026) - 773644000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624937024) - 773644000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624938025) - 773644000 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624939022) - 773644000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624940024) - 773644000 -> 56759000 (116680003) View
116680003 \|Is a (attribute)\|	56759000 \|Congenital anomaly of subcutaneous tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624941023) - 773644000 -> 399959003 (116680003) View
116680003 \|Is a (attribute)\|	399959003 \|Premature aging syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624942027) - 773644000 -> 89545001 (363698007) View
363698007 \|Finding site (attribute)\|	89545001 \|Face structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624943021) - 773644000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624944026) - 773644000 -> 67769002 (363698007) View
363698007 \|Finding site (attribute)\|	67769002 \|Structure of subcutaneous fatty tissue (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624945025) - 773644000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624946029) - 773644000 -> 19346006 (116680003) View
116680003 \|Is a (attribute)\|	19346006 \|Marfan's syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624947022) - 773644000 -> 724841000 (116680003) View
116680003 \|Is a (attribute)\|	724841000 \|Genetic lipodystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
724841000 View
724841000	Genetic lipodystrophy (disorder)	Genetic lipodystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363039000 View
363039000	Congenital connective tissue disorder (disorder)	Congenital connective tissue disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
399959003 View
399959003	Premature aging syndrome (disorder)	Premature aging syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
19346006 View
19346006	Marfan's syndrome (disorder)	Marfan syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
56759000 View
56759000	Congenital anomaly of subcutaneous tissue (disorder)	Congenital anomaly of subcutaneous tissue	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
65094009 View
65094009	Multiple malformation syndrome with facial defects as major feature (disorder)	Multiple malformation syndrome with facial defects as major feature	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 (a2772c7b-a9d5-55f1-80ad-3b08540b2bbd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.1	TRUE	ALWAYS E88.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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