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Terminology chevron_right Concepts chevron_right 235730004

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Component

235730004

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial absence of villi (disorder)

Shortest Term

Familial absence of villi

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

Familial absence of villi (disorder)

SCTID: 235730004, Primitive, Active

235730004|Familial absence of villi (disorder)|

en Familial absence of villi
en Familial absence of villi (disorder)

Expression

235730004 |Familial absence of villi (disorder)|
 <<< 235729009 |Congenital microvillous atrophy (disorder)| + 
111941005 |Familial disease (disorder)| + 
897442002 |Structural abnormality of small intestinal villus (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 125471000 |Microvillus alteration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 23230007 |Intestinal villus (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
353383018 - Familial absence of villi (en) View
353383018	en	Synonym (core metadata concept)	Familial absence of villi	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
624227015 - Familial absence of villi (disorder) (en) View
624227015	en	Fully specified name (core metadata concept)	Familial absence of villi (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12065278024) - 235730004 -> 128068002 (116680003) View
116680003 \|Is a (attribute)\|	128068002 \|Disorder of gastrointestinal tract mucous membrane (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16205212026) - 235730004 -> 280130008 (116680003) View
116680003 \|Is a (attribute)\|	280130008 \|Disorder of soft tissue of abdominal cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16381697022) - 235730004 -> 897442002 (116680003) View
116680003 \|Is a (attribute)\|	897442002 \|Structural abnormality of small intestinal villus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12065282021) - 235730004 -> 280133005 (116680003) View
116680003 \|Is a (attribute)\|	280133005 \|Disorder of soft tissue of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (50335027) - 235730004 -> 55193002 (116680003) View
116680003 \|Is a (attribute)\|	55193002 \|Congenital anomaly of small intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3392628024) - 235730004 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010780023) - 235730004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010781022) - 235730004 -> 125471000 (116676008) View
116676008 \|Associated morphology (attribute)\|	125471000 \|Microvillus alteration (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010782026) - 235730004 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10530134029) - 235730004 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065279027) - 235730004 -> 23230007 (363698007) View
363698007 \|Finding site (attribute)\|	23230007 \|Intestinal villus (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12065280029) - 235730004 -> 125471000 (116676008) View
116676008 \|Associated morphology (attribute)\|	125471000 \|Microvillus alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12065281025) - 235730004 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3392629027) - 235730004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4972668027) - 235730004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4972669024) - 235730004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989685022) - 235730004 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10530132025) - 235730004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530133024) - 235730004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2574407020) - 235730004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (519636024) - 235730004 -> 30315005 (363698007) View
363698007 \|Finding site (attribute)\|	30315005 \|Small intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1728512027) - 235730004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1728513021) - 235730004 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (519635023) - 235730004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (50336026) - 235730004 -> 235729009 (116680003) View
116680003 \|Is a (attribute)\|	235729009 \|Congenital microvillous atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
897442002 View
897442002	Structural abnormality of small intestinal villus (disorder)	Abnormal small intestinal villus morphology	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
111941005 View
111941005	Familial disease (disorder)	Familial disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
235729009 View
235729009	Congenital microvillous atrophy (disorder)	Davidson disease	900000000000074008 \|Necessary but not sufficient concept 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 (35b5e457-d993-507c-9dea-e7123312af52) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q43.8	TRUE	ALWAYS Q43.8	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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