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Terminology chevron_right Concepts chevron_right 15419008

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Component

15419008

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital pyloric membrane (disorder)

Shortest Term

Congenital pyloric membrane

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Congenital pyloric membrane (disorder)

SCTID: 15419008, Defined, Active

15419008|Congenital pyloric membrane (disorder)|

en Congenital pyloric membrane
en Congenital pyloric membrane (disorder)

Expression

15419008 |Congenital pyloric membrane (disorder)|
 === 60699003 |Congenital anomaly of stomach (disorder)| + 
300296006 |Lesion of stomach (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 76640006 |Congenital webbing (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 280119005 |Pyloric structure of stomach (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
26147010 - Congenital pyloric membrane (en) View
26147010	en	Synonym (core metadata concept)	Congenital pyloric membrane	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
742235012 - Congenital pyloric membrane (disorder) (en) View
742235012	en	Fully specified name (core metadata concept)	Congenital pyloric membrane (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (707844023) - 15419008 -> 76640006 (116676008) View
116676008 \|Associated morphology (attribute)\|	76640006 \|Congenital webbing (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3400114023) - 15419008 -> 280119005 (363698007) View
363698007 \|Finding site (attribute)\|	280119005 \|Pyloric structure of stomach (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5862750025) - 15419008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6072779024) - 15419008 -> 76640006 (116676008) View
116676008 \|Associated morphology (attribute)\|	76640006 \|Congenital webbing (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6072780022) - 15419008 -> 280119005 (363698007) View
363698007 \|Finding site (attribute)\|	280119005 \|Pyloric structure of stomach (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10519131023) - 15419008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10519132027) - 15419008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3467045028) - 15419008 -> 76640006 (116676008) View
116676008 \|Associated morphology (attribute)\|	76640006 \|Congenital webbing (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4990345025) - 15419008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4990346029) - 15419008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4990347022) - 15419008 -> 69695003 (363698007) View
363698007 \|Finding site (attribute)\|	69695003 \|Stomach structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5978760029) - 15419008 -> 300296006 (116680003) View
116680003 \|Is a (attribute)\|	300296006 \|Lesion of stomach (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2591234026) - 15419008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3172078028) - 15419008 -> 128347007 (116680003) View
116680003 \|Is a (attribute)\|	128347007 \|Congenital anomaly of gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3179203026) - 15419008 -> 363024001 (116680003) View
116680003 \|Is a (attribute)\|	363024001 \|Congenital anomaly of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3771561022) - 15419008 -> 275262008 (116680003) View
116680003 \|Is a (attribute)\|	275262008 \|Congenital malformation of upper alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3181349026) - 15419008 -> 363026004 (116680003) View
116680003 \|Is a (attribute)\|	363026004 \|Congenital anomaly of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1757796027) - 15419008 -> 280119005 (363698007) View
363698007 \|Finding site (attribute)\|	280119005 \|Pyloric structure of stomach (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2544038022) - 15419008 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (707845024) - 15419008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (707846020) - 15419008 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1757795028) - 15419008 -> 51289009 (363698007) View
363698007 \|Finding site (attribute)\|	51289009 \|Digestive tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1757797020) - 15419008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (171132027) - 15419008 -> 335002 (116680003) View
116680003 \|Is a (attribute)\|	335002 \|Pylorospasm (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (707847027) - 15419008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (707848021) - 15419008 -> 78987009 (363698007) View
363698007 \|Finding site (attribute)\|	78987009 \|Pylorus structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (171133021) - 15419008 -> 60699003 (116680003) View
116680003 \|Is a (attribute)\|	60699003 \|Congenital anomaly of stomach (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
300296006 View
300296006	Lesion of stomach (disorder)	Lesion of stomach	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60699003 View
60699003	Congenital anomaly of stomach (disorder)	Congenital anomaly of stomach	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 (a45948fe-1b96-52be-b0cc-1bfdac41d1cd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q40.2	TRUE	ALWAYS Q40.2	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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