dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 55824003

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Essential benign pentosuria (disorder)

Shortest Term

Pentosuria

Definition Status

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

Summary

Essential benign pentosuria (disorder)

SCTID: 55824003, Primitive, Inactive

55824003|Essential benign pentosuria (disorder)|

Expression

55824003 |Essential benign pentosuria (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
92832010 - Essential benign pentosuria (en) View
92832010	en	Synonym (core metadata concept)	Essential benign pentosuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
794253018 - Essential benign pentosuria (disorder) (en) View
794253018	en	Fully specified name (core metadata concept)	Essential benign pentosuria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
92833017 - Pentosuria (en) View
92833017	en	Synonym (core metadata concept)	Pentosuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
92835012 - L-xylulose reductase deficiency (en) View
92835012	en	Synonym (core metadata concept)	L-xylulose reductase deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
92836013 - L-xylulosuria (en) View
92836013	en	Synonym (core metadata concept)	L-xylulosuria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
92834011 - Xylitol dehydrogenase deficiency (en) View
92834011	en	Synonym (core metadata concept)	Xylitol dehydrogenase deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (238878023) - 55824003 -> 78548001 (116680003) View
116680003 \|Is a (attribute)\|	78548001 \|Enzymopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238879026) - 55824003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238880028) - 55824003 -> 57507002 (116680003) View
116680003 \|Is a (attribute)\|	57507002 \|Pentose disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238881029) - 55824003 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812505021) - 55824003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812504020) - 55824003 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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

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

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (238878023) - 55824003 -> 78548001 (116680003) View
116680003 \|Is a (attribute)\|	78548001 \|Enzymopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238879026) - 55824003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238880028) - 55824003 -> 57507002 (116680003) View
116680003 \|Is a (attribute)\|	57507002 \|Pentose disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238881029) - 55824003 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812505021) - 55824003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812504020) - 55824003 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Descriptions