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Terminology chevron_right Concepts chevron_right 20756002

Production

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Component

20756002

The component that hold information about this concept.

Fully Specified Name (FSN)

Adult hypophosphatasia (disorder)

Shortest Term

Adult hypophosphatasia

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

Adult hypophosphatasia (disorder)

SCTID: 20756002, Primitive, Active

20756002|Adult hypophosphatasia (disorder)|

en Adult hypophosphatasia
en Adult hypophosphatasia (disorder)
en Hypophosphatasia, adult type

Expression

20756002 |Adult hypophosphatasia (disorder)|
 <<< 78548001 |Enzymopathy (disorder)| + 
190859005 |Hypophosphatasia (disorder)| + 
1899006 |Autosomal hereditary disorder (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 41847000 |Adulthood (qualifier value)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
34921013 - Adult hypophosphatasia (en) View
34921013	en	Synonym (core metadata concept)	Adult hypophosphatasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
749974011 - Adult hypophosphatasia (disorder) (en) View
749974011	en	Fully specified name (core metadata concept)	Adult hypophosphatasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
34922018 - Hypophosphatasia, adult type (en) View
34922018	en	Synonym (core metadata concept)	Hypophosphatasia, adult type	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (724369027) - 20756002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (724371027) - 20756002 -> 41847000 (246454002) View
246454002 \|Occurrence (attribute)\|	41847000 \|Adulthood (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (724370026) - 20756002 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (181961021) - 20756002 -> 78548001 (116680003) View
116680003 \|Is a (attribute)\|	78548001 \|Enzymopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (181962025) - 20756002 -> 190859005 (116680003) View
116680003 \|Is a (attribute)\|	190859005 \|Hypophosphatasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (181963024) - 20756002 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1899006 View
1899006	Autosomal hereditary disorder (disorder)	Autosomal hereditary disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
78548001 View
78548001	Enzymopathy (disorder)	Enzymopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
190859005 View
190859005	Hypophosphatasia (disorder)	Hypophosphatasia	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 (d6071ec0-dcf9-5e80-b864-080443798bd1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.3	TRUE	ALWAYS E83.3	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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