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Terminology chevron_right Concepts chevron_right 69478001

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Component

69478001

The component that hold information about this concept.

Fully Specified Name (FSN)

Pancreatic colipase deficiency (disorder)

Shortest Term

Thiếu colipase tuyến tụy

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

Pancreatic colipase deficiency (disorder)

SCTID: 69478001, Primitive, Active

69478001|Pancreatic colipase deficiency (disorder)|

vi Thiếu colipase tuyến tụy
en Pancreatic colipase deficiency
en Pancreatic colipase deficiency (disorder)

Expression

69478001 |Pancreatic colipase deficiency (disorder)|
 <<< 42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| + 
78548001 |Enzymopathy (disorder)| + 
86095007 |Inborn error of metabolism (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
302920007 |Pancreatic malabsorption (disorder)| : 
        { 363698007 |Finding site (attribute)| = 30315005 |Small intestinal structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 15776009 |Pancreatic structure (body structure)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
441411000003119 - thiếu colipase tuyến tụy (vi) View
441411000003119	vi	Synonym (core metadata concept)	thiếu colipase tuyến tụy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
115426011 - Pancreatic colipase deficiency (en) View
115426011	en	Synonym (core metadata concept)	Pancreatic colipase deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
809427011 - Pancreatic colipase deficiency (disorder) (en) View
809427011	en	Fully specified name (core metadata concept)	Pancreatic colipase deficiency (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880823023) - 69478001 -> 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 (12876677023) - 69478001 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (847267029) - 69478001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5045372024) - 69478001 -> 15776009 (363698007) View
363698007 \|Finding site (attribute)\|	15776009 \|Pancreatic structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5045373025) - 69478001 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1680663026) - 69478001 -> 46842007 (116680003) View
116680003 \|Is a (attribute)\|	46842007 \|Congenital anomaly of pancreas (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2695831021) - 69478001 -> 55193002 (116680003) View
116680003 \|Is a (attribute)\|	55193002 \|Congenital anomaly of small intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3348056023) - 69478001 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3348057025) - 69478001 -> 15776009 (363698007) View
363698007 \|Finding site (attribute)\|	15776009 \|Pancreatic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3445401028) - 69478001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (847268023) - 69478001 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (847269026) - 69478001 -> 15776009 (363698007) View
363698007 \|Finding site (attribute)\|	15776009 \|Pancreatic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1775853027) - 69478001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2230560027) - 69478001 -> 95470009 (116680003) View
116680003 \|Is a (attribute)\|	95470009 \|Congenital anomaly of digestive tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1775851025) - 69478001 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1775852021) - 69478001 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2039932028) - 69478001 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1775850029) - 69478001 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (261062022) - 69478001 -> 32230006 (116680003) View
116680003 \|Is a (attribute)\|	32230006 \|Malabsorption syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (261064023) - 69478001 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (261065024) - 69478001 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (261066020) - 69478001 -> 3855007 (116680003) View
116680003 \|Is a (attribute)\|	3855007 \|Disorder of pancreas (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (261067027) - 69478001 -> 238017009 (116680003) View
116680003 \|Is a (attribute)\|	238017009 \|Disorder of lipid storage and metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1680662020) - 69478001 -> 302920007 (116680003) View
116680003 \|Is a (attribute)\|	302920007 \|Pancreatic malabsorption (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1680664021) - 69478001 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (261061026) - 69478001 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (261063028) - 69478001 -> 78548001 (116680003) View
116680003 \|Is a (attribute)\|	78548001 \|Enzymopathy (disorder)\|	0	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
78548001 View
78548001	Enzymopathy (disorder)	Enzymopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
86095007 View
86095007	Inborn error of metabolism (disorder)	Inborn error of metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
302920007 View
302920007	Pancreatic malabsorption (disorder)	Kém hấp thu do tụ	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
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	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 (5530c954-e647-52a0-bd5d-97735396d1fa) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E75.5	TRUE	ALWAYS E75.5	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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