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Terminology chevron_right Concepts chevron_right 83145004

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Component

83145004

The component that hold information about this concept.

Fully Specified Name (FSN)

Abnormal dermatoglyphic pattern (disorder)

Shortest Term

Dermatoglyphic anomalies

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

Abnormal dermatoglyphic pattern (disorder)

SCTID: 83145004, Defined, Active

83145004|Abnormal dermatoglyphic pattern (disorder)|

en Abnormal dermatoglyphic pattern
en Abnormal dermatoglyphic pattern (disorder)
en Dermatoglyphic abnormality
en Dermatoglyphic anomalies

Expression

83145004 |Abnormal dermatoglyphic pattern (disorder)|
 === 199879009 |Congenital anomaly of skin (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (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
137907016 - Abnormal dermatoglyphic pattern (en) View
137907016	en	Synonym (core metadata concept)	Abnormal dermatoglyphic pattern	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
824717012 - Abnormal dermatoglyphic pattern (disorder) (en) View
824717012	en	Fully specified name (core metadata concept)	Abnormal dermatoglyphic pattern (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
505464012 - Dermatoglyphic abnormality (en) View
505464012	en	Synonym (core metadata concept)	Dermatoglyphic abnormality	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
505463018 - Dermatoglyphic anomalies (en) View
505463018	en	Synonym (core metadata concept)	Dermatoglyphic anomalies	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (882170026) - 83145004 -> 42235004 (363698007) View
363698007 \|Finding site (attribute)\|	42235004 \|Structure of dermatoglyphic patterns (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971279026) - 83145004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4971280028) - 83145004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017309021) - 83145004 -> 42235004 (363698007) View
363698007 \|Finding site (attribute)\|	42235004 \|Structure of dermatoglyphic patterns (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6089394025) - 83145004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517748029) - 83145004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517749021) - 83145004 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (882169027) - 83145004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3359911026) - 83145004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3445741020) - 83145004 -> 42235004 (363698007) View
363698007 \|Finding site (attribute)\|	42235004 \|Structure of dermatoglyphic patterns (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1780261022) - 83145004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (882171027) - 83145004 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (283265025) - 83145004 -> 199879009 (116680003) View
116680003 \|Is a (attribute)\|	199879009 \|Congenital anomaly of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
199879009 View
199879009	Congenital anomaly of skin (disorder)	Genodermatosis, nos	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
763748007 View
763748007	Isolated congenital adermatoglyphia (disorder)	Immigration delay disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719595002 View
719595002	Absence of fingerprints with congenital milia syndrome (disorder)	Baird syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
95469008 View
95469008	Abnormal plantar creases (disorder)	Abnormal plantar creases	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
165185004 View
165185004	Dermatoglyphs - skin lines (disorder)	Skin lines	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
205557000 View
205557000	Abnormal palmar creases (disorder)	Abnormal palmar creases	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (963d56c2-a20b-5b5f-8ba8-0747a18cd228) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8	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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