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Terminology chevron_right Concepts chevron_right 722392003

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Component

722392003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)

Shortest Term

Enteric anendocrinosis

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 malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)

SCTID: 722392003, Primitive, Active

722392003|Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)|

en Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
en Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)
en Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells
en Enteric anendocrinosis

Expression

722392003 |Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)|
 <<< 25319005 |Chronic diarrhea of infants and/or young children (disorder)| + 
32230006 |Malabsorption syndrome (disorder)| + 
66091009 |Congenital disease (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| : 
        { 363698007 |Finding site (attribute)| = 113276009 |Intestinal structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 122865005 |Gastrointestinal tract structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 90734009 |Chronic (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3326711011 - Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (en) View
3326711011	en	Synonym (core metadata concept)	Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3326710012 - Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) (en) View
3326710012	en	Fully specified name (core metadata concept)	Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3331831014 - Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells (en) View
3331831014	en	Synonym (core metadata concept)	Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3331832019 - Enteric anendocrinosis (en) View
3331832019	en	Synonym (core metadata concept)	Enteric anendocrinosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880914024) - 722392003 -> 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 (9280851022) - 722392003 -> 39211005 (363714003) View
363714003 \|Interprets (attribute)\|	39211005 \|Bowel action (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9280852026) - 722392003 -> 18307000 (363713009) View
363713009 \|Has interpretation (attribute)\|	18307000 \|Altered (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13719077021) - 722392003 -> 106079008 (363714003) View
363714003 \|Interprets (attribute)\|	106079008 \|Digestive system function (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6779145022) - 722392003 -> 90734009 (263502005) View
263502005 \|Clinical course (attribute)\|	90734009 \|Chronic (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9280850023) - 722392003 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6779146023) - 722392003 -> 62315008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62315008 \|Diarrhea (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6779140028) - 722392003 -> 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 (6779141029) - 722392003 -> 32230006 (116680003) View
116680003 \|Is a (attribute)\|	32230006 \|Malabsorption syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6779142020) - 722392003 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6779143026) - 722392003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6779144021) - 722392003 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6779147025) - 722392003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6779148024) - 722392003 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	3	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
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 (ffa97c90-ce84-53b6-8b0e-cd68404f38a5) 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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