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Terminology chevron_right Concepts chevron_right 719595002

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Component

719595002

The component that hold information about this concept.

Fully Specified Name (FSN)

Absence of fingerprints with congenital milia syndrome (disorder)

Shortest Term

Baird syndrome

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

Absence of fingerprints with congenital milia syndrome (disorder)

SCTID: 719595002, Primitive, Active

719595002|Absence of fingerprints with congenital milia syndrome (disorder)|

en Absence of dermatoglyphics with congenital milia syndrome
en Absence of fingerprints with congenital milia syndrome
en Absence of fingerprints with congenital milia syndrome (disorder)
en Baird syndrome

Expression

719595002 |Absence of fingerprints with congenital milia syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
83145004 |Abnormal dermatoglyphic pattern (disorder)| + 
254679001 |Milia (disorder)| + 
363185004 |Hereditary disorder of the integument (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 37719003 |Milium (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 42235004 |Structure of dermatoglyphic patterns (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
3317078012 - Absence of dermatoglyphics with congenital milia syndrome (en) View
3317078012	en	Synonym (core metadata concept)	Absence of dermatoglyphics with congenital milia syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3317077019 - Absence of fingerprints with congenital milia syndrome (en) View
3317077019	en	Synonym (core metadata concept)	Absence of fingerprints with congenital milia syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3317076011 - Absence of fingerprints with congenital milia syndrome (disorder) (en) View
3317076011	en	Fully specified name (core metadata concept)	Absence of fingerprints with congenital milia syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3317079016 - Baird syndrome (en) View
3317079016	en	Synonym (core metadata concept)	Baird syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6640673024) - 719595002 -> 254237003 (116680003) View
116680003 \|Is a (attribute)\|	254237003 \|Aplasia of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6641776025) - 719595002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069175022) - 719595002 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13180400022) - 719595002 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6640676027) - 719595002 -> 702626005 (116680003) View
116680003 \|Is a (attribute)\|	702626005 \|Congenital absence (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6640677020) - 719595002 -> 37719003 (116676008) View
116676008 \|Associated morphology (attribute)\|	37719003 \|Milium (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6640679023) - 719595002 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6640680021) - 719595002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6640681020) - 719595002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6640682029) - 719595002 -> 42235004 (363698007) View
363698007 \|Finding site (attribute)\|	42235004 \|Structure of dermatoglyphic patterns (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6641777023) - 719595002 -> 42235004 (363698007) View
363698007 \|Finding site (attribute)\|	42235004 \|Structure of dermatoglyphic patterns (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517751020) - 719595002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517752029) - 719595002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517754028) - 719595002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10538126023) - 719595002 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10538127025) - 719595002 -> 37719003 (116676008) View
116676008 \|Associated morphology (attribute)\|	37719003 \|Milium (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6640671021) - 719595002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6640672025) - 719595002 -> 83145004 (116680003) View
116680003 \|Is a (attribute)\|	83145004 \|Abnormal dermatoglyphic pattern (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6640674029) - 719595002 -> 254679001 (116680003) View
116680003 \|Is a (attribute)\|	254679001 \|Milia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6640675028) - 719595002 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6640678026) - 719595002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
83145004 View
83145004	Abnormal dermatoglyphic pattern (disorder)	Dermatoglyphic anomalies	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
254679001 View
254679001	Milia (disorder)	Milia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363185004 View
363185004	Hereditary disorder of the integument (disorder)	Hereditary disorder of the integument	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 (b5173c7d-42fc-52d0-86fe-f3eb0f78d4c0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8 \| 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)\|

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