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Terminology chevron_right Concepts chevron_right 237965005

Production

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Component

237965005

The component that hold information about this concept.

Fully Specified Name (FSN)

Phosphate transport defect (disorder)

Shortest Term

Phosphate transport defect

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

Phosphate transport defect (disorder)

SCTID: 237965005, Primitive, Active

237965005|Phosphate transport defect (disorder)|

en Phosphate transport defect
en Phosphate transport defect (disorder)
en Glycogen storage disease type ic

Expression

237965005 |Phosphate transport defect (disorder)|
 <<< 29633007 |Glycogen storage disease (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
356654017 - Phosphate transport defect (en) View
356654017	en	Synonym (core metadata concept)	Phosphate transport defect	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626776012 - Phosphate transport defect (disorder) (en) View
626776012	en	Fully specified name (core metadata concept)	Phosphate transport defect (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
356653011 - Glycogen storage disease type Ic (en) View
356653011	en	Synonym (core metadata concept)	Glycogen storage disease type Ic	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (526951026) - 237965005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2476994024) - 237965005 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526952022) - 237965005 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526953028) - 237965005 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53597021) - 237965005 -> 29633007 (116680003) View
116680003 \|Is a (attribute)\|	29633007 \|Glycogen storage disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
29633007 View
29633007	Glycogen storage disease (disorder)	Glycogenosis	900000000000073002 \|Sufficiently defined by necessary conditions 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 (d495724a-dd45-5ce4-b9d3-dbd65bd563a3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E74.0	TRUE	ALWAYS E74.0	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)\|

Terminology chevron_right Concepts chevron_right 237965005

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