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Terminology chevron_right Concepts chevron_right 24412005

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Component

24412005

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital secretory diarrhea, chloride type (disorder)

Shortest Term

Congenital chloridorrhea

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

Congenital secretory diarrhea, chloride type (disorder)

SCTID: 24412005, Primitive, Active

24412005|Congenital secretory diarrhea, chloride type (disorder)|

en Congenital chloride diarrhea
en Congenital chloride diarrhoea
en Congenital chloridorrhea
en Congenital chloridorrhoea
en Congenital secretory diarrhea, chloride type
en Congenital secretory diarrhea, chloride type (disorder)
en Congenital secretory diarrhoea, chloride type
en Defective cl^-^/hco^-^>3< exchange in ileum and/or colon

Expression

24412005 |Congenital secretory diarrhea, chloride type (disorder)|
 <<< 25898005 |Congenital secretory diarrhea (disorder)| + 
32230006 |Malabsorption syndrome (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 14742008 |Large intestinal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 18307000 |Altered (qualifier value)|,
363714003 |Interprets (attribute)| = 39211005 |Bowel action (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4545036014 - Congenital chloride diarrhea (en) View
4545036014	en	Synonym (core metadata concept)	Congenital chloride diarrhea	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4545035013 - Congenital chloride diarrhoea (en) View
4545035013	en	Synonym (core metadata concept)	Congenital chloride diarrhoea	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
40947013 - Congenital chloridorrhea (en) View
40947013	en	Synonym (core metadata concept)	Congenital chloridorrhea	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
481907012 - Congenital chloridorrhoea (en) View
481907012	en	Synonym (core metadata concept)	Congenital chloridorrhoea	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
40946016 - Congenital secretory diarrhea, chloride type (en) View
40946016	en	Synonym (core metadata concept)	Congenital secretory diarrhea, chloride type	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
754046012 - Congenital secretory diarrhea, chloride type (disorder) (en) View
754046012	en	Fully specified name (core metadata concept)	Congenital secretory diarrhea, chloride type (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
481908019 - Congenital secretory diarrhoea, chloride type (en) View
481908019	en	Synonym (core metadata concept)	Congenital secretory diarrhoea, chloride type	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
40948015 - Defective Cl^-^/HCO^-^>3< exchange in ileum and colon (en) View
40948015	en	Synonym (core metadata concept)	Defective Cl^-^/HCO^-^>3< exchange in ileum and colon	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
40949011 - Defective Cl^-^/HCO^-^>3< exchange in ileum AND/OR colon (en) View
40949011	en	Synonym (core metadata concept)	Defective Cl^-^/HCO^-^>3< exchange in ileum AND/OR colon	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13718904020) - 24412005 -> 106079008 (363714003) View
363714003 \|Interprets (attribute)\|	106079008 \|Digestive system function (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13675313028) - 24412005 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13675314023) - 24412005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (733513021) - 24412005 -> 62315008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62315008 \|Diarrhea (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7599828023) - 24412005 -> 18307000 (363713009) View
363713009 \|Has interpretation (attribute)\|	18307000 \|Altered (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7599829026) - 24412005 -> 39211005 (363714003) View
363714003 \|Interprets (attribute)\|	39211005 \|Bowel action (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (733514026) - 24412005 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2592800020) - 24412005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5013196028) - 24412005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5013197021) - 24412005 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (733512027) - 24412005 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (187811021) - 24412005 -> 25898005 (116680003) View
116680003 \|Is a (attribute)\|	25898005 \|Congenital secretory diarrhea (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (187812025) - 24412005 -> 32230006 (116680003) View
116680003 \|Is a (attribute)\|	32230006 \|Malabsorption syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
25898005 View
25898005	Congenital secretory diarrhea (disorder)	Congenital secretory diarrhea	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
32230006 View
32230006	Malabsorption syndrome (disorder)	Malabsorption	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	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 (b5da621d-99f6-5033-9e26-872c44d883ae) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K52.8	TRUE	ALWAYS K52.8	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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