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Terminology chevron_right Concepts chevron_right 763748007

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Component

763748007

The component that hold information about this concept.

Fully Specified Name (FSN)

Isolated congenital adermatoglyphia (disorder)

Shortest Term

Immigration delay disease

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

Isolated congenital adermatoglyphia (disorder)

SCTID: 763748007, Primitive, Active

763748007|Isolated congenital adermatoglyphia (disorder)|

en Congenital absence of fingerprints
en Immigration delay disease
en Isolated congenital adermatoglyphia
en Isolated congenital adermatoglyphia (disorder)

Expression

763748007 |Isolated congenital adermatoglyphia (disorder)|
 <<< 363185004 |Hereditary disorder of the integument (disorder)| + 
83145004 |Abnormal dermatoglyphic pattern (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 314292007 |Entire 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
3643623016 - Congenital absence of fingerprints (en) View
3643623016	en	Synonym (core metadata concept)	Congenital absence of fingerprints	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3643626012 - Immigration delay disease (en) View
3643626012	en	Synonym (core metadata concept)	Immigration delay disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3643622014 - Isolated congenital adermatoglyphia (en) View
3643622014	en	Synonym (core metadata concept)	Isolated congenital adermatoglyphia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3643624010 - Isolated congenital adermatoglyphia (disorder) (en) View
3643624010	en	Fully specified name (core metadata concept)	Isolated congenital adermatoglyphia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9132212027) - 763748007 -> 254237003 (116680003) View
116680003 \|Is a (attribute)\|	254237003 \|Aplasia of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9132215025) - 763748007 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069909025) - 763748007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13182732027) - 763748007 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132214026) - 763748007 -> 702626005 (116680003) View
116680003 \|Is a (attribute)\|	702626005 \|Congenital absence (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10526748022) - 763748007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132210024) - 763748007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132211023) - 763748007 -> 83145004 (116680003) View
116680003 \|Is a (attribute)\|	83145004 \|Abnormal dermatoglyphic pattern (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132213021) - 763748007 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132216029) - 763748007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9132217022) - 763748007 -> 314292007 (363698007) View
363698007 \|Finding site (attribute)\|	314292007 \|Entire dermatoglyphic patterns (body structure)\|	1	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
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 (f9718e2a-04cd-5eae-9e6d-3bd93929ed25) 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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