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Terminology chevron_right Concepts chevron_right 65764006

Production

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Component

65764006

The component that hold information about this concept.

Fully Specified Name (FSN)

Pseudo-hurler polydystrophy (disorder)

Shortest Term

Mucolipidosis iii

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

Pseudo-hurler polydystrophy (disorder)

SCTID: 65764006, Primitive, Active

65764006|Pseudo-hurler polydystrophy (disorder)|

en Pseudo-hurler's disease
en Mucolipidosis iii
en Pseudo-hurler disease
en Pseudo-hurler polydystrophy
en Pseudo-hurler polydystrophy (disorder)

Expression

65764006 |Pseudo-hurler polydystrophy (disorder)|
 <<< 70199000 |I-cell disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 272673000 |Bone 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
1232722017 - Pseudo-Hurler's disease (en) View
1232722017	en	Synonym (core metadata concept)	Pseudo-Hurler's disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
109252017 - Mucolipidosis III (en) View
109252017	en	Synonym (core metadata concept)	Mucolipidosis III	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
109253010 - Pseudo-Hurler disease (en) View
109253010	en	Synonym (core metadata concept)	Pseudo-Hurler disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
109251012 - Pseudo-Hurler polydystrophy (en) View
109251012	en	Synonym (core metadata concept)	Pseudo-Hurler polydystrophy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
805303019 - Pseudo-Hurler polydystrophy (disorder) (en) View
805303019	en	Fully specified name (core metadata concept)	Pseudo-Hurler polydystrophy (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (837848023) - 65764006 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3384328025) - 65764006 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (837845021) - 65764006 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4980119028) - 65764006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989852027) - 65764006 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5023430027) - 65764006 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10533834028) - 65764006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10533835027) - 65764006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (837846022) - 65764006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3384329022) - 65764006 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1774521021) - 65764006 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (837847029) - 65764006 -> 113192009 (363698007) View
363698007 \|Finding site (attribute)\|	113192009 \|Skeletal system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (255039029) - 65764006 -> 70199000 (116680003) View
116680003 \|Is a (attribute)\|	70199000 \|I-cell disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
70199000 View
70199000	I-cell disease (disorder)	I-cell disease	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 (2a43020c-ba96-5031-bc91-a417cd3b0c07) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E76.0	TRUE	ALWAYS E76.0	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 (f8c1cbb7-9840-5850-b2bd-864891c470f3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E77.0	TRUE	ALWAYS E77.0	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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