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Terminology chevron_right Concepts chevron_right 773579007

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Component

773579007

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital chronic diarrhea with protein-losing enteropathy (disorder)

Shortest Term

Congenital chronic diarrhea with exudative enteropathy

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 chronic diarrhea with protein-losing enteropathy (disorder)

SCTID: 773579007, Primitive, Active

773579007|Congenital chronic diarrhea with protein-losing enteropathy (disorder)|

en Congenital chronic diarrhea with exudative enteropathy
en Congenital chronic diarrhea with protein-losing enteropathy
en Congenital chronic diarrhea with protein-losing enteropathy (disorder)
en Congenital chronic diarrhoea with exudative enteropathy
en Congenital chronic diarrhoea with protein-losing enteropathy

Expression

773579007 |Congenital chronic diarrhea with protein-losing enteropathy (disorder)|
 <<< 42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| + 
25319005 |Chronic diarrhea of infants and/or young children (disorder)| + 
66091009 |Congenital disease (disorder)| + 
66972006 |Protein-losing enteropathy (disorder)| + 
128333008 |Diarrheal disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 30315005 |Small 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)| }
        { 263502005 |Clinical course (attribute)| = 90734009 |Chronic (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3724273012 - Congenital chronic diarrhea with exudative enteropathy (en) View
3724273012	en	Synonym (core metadata concept)	Congenital chronic diarrhea with exudative enteropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3724275017 - Congenital chronic diarrhea with protein-losing enteropathy (en) View
3724275017	en	Synonym (core metadata concept)	Congenital chronic diarrhea with protein-losing enteropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3724272019 - Congenital chronic diarrhea with protein-losing enteropathy (disorder) (en) View
3724272019	en	Fully specified name (core metadata concept)	Congenital chronic diarrhea with protein-losing enteropathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3724276016 - Congenital chronic diarrhoea with exudative enteropathy (en) View
3724276016	en	Synonym (core metadata concept)	Congenital chronic diarrhoea with exudative enteropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3724274018 - Congenital chronic diarrhoea with protein-losing enteropathy (en) View
3724274018	en	Synonym (core metadata concept)	Congenital chronic diarrhoea with protein-losing enteropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880899025) - 773579007 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15780770026) - 773579007 -> 128333008 (116680003) View
116680003 \|Is a (attribute)\|	128333008 \|Diarrheal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13719068025) - 773579007 -> 106079008 (363714003) View
363714003 \|Interprets (attribute)\|	106079008 \|Digestive system function (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10607242022) - 773579007 -> 90734009 (263502005) View
263502005 \|Clinical course (attribute)\|	90734009 \|Chronic (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607240025) - 773579007 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607241026) - 773579007 -> 39211005 (363714003) View
363714003 \|Interprets (attribute)\|	39211005 \|Bowel action (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607243028) - 773579007 -> 18307000 (363713009) View
363713009 \|Has interpretation (attribute)\|	18307000 \|Altered (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607244023) - 773579007 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607245024) - 773579007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607246020) - 773579007 -> 25319005 (116680003) View
116680003 \|Is a (attribute)\|	25319005 \|Chronic diarrhea of infants and/or young children (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607247027) - 773579007 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607248021) - 773579007 -> 66972006 (116680003) View
116680003 \|Is a (attribute)\|	66972006 \|Protein-losing enteropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10607249029) - 773579007 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
25319005 View
25319005	Chronic diarrhea of infants and/or young children (disorder)	Chronic diarrhea of infants and young children	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
66972006 View
66972006	Protein-losing enteropathy (disorder)	Protein-losing enteropathy	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
128333008 View
128333008	Diarrheal disorder (disorder)	Diarrhea disorder	900000000000073002 \|Sufficiently defined by necessary conditions 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 (07d62ef8-f92a-5545-b4c1-10a4fc8f0807) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K90.4	TRUE	ALWAYS K90.4	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 (9c82a882-5597-5822-a7fd-426431869e12) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K52.8	TRUE	ALWAYS K52.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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 (d0a83e91-ab69-55b3-a10b-9c2f24435ff2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P78.3	TRUE	ALWAYS P78.3 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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