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Terminology chevron_right Concepts chevron_right 763368004

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Component

763368004

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)

Shortest Term

Familial progressive hyper and hypopigmentation

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 progressive hyperpigmentation and hypopigmentation of skin (disorder)

SCTID: 763368004, Primitive, Active

763368004|Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)|

en Familial progressive hyper and hypopigmentation
en Familial progressive hyperpigmentation and hypopigmentation of skin
en Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)

Expression

763368004 |Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
205564003 |Congenital pigmentary skin anomalies (disorder)| + 
724839001 |Genetic disorder of skin pigmentation (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
363185004 |Hereditary disorder of the integument (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 79644001 |Pigment alteration (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)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3640241016 - Familial progressive hyper and hypopigmentation (en) View
3640241016	en	Synonym (core metadata concept)	Familial progressive hyper and hypopigmentation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3640240015 - Familial progressive hyperpigmentation and hypopigmentation of skin (en) View
3640240015	en	Synonym (core metadata concept)	Familial progressive hyperpigmentation and hypopigmentation of skin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3640242011 - Familial progressive hyperpigmentation and hypopigmentation of skin (disorder) (en) View
3640242011	en	Fully specified name (core metadata concept)	Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15392702023) - 763368004 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069898028) - 763368004 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9102392027) - 763368004 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9102393021) - 763368004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9102394026) - 763368004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9224403024) - 763368004 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9238804020) - 763368004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10514663027) - 763368004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9102389026) - 763368004 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9102390024) - 763368004 -> 205564003 (116680003) View
116680003 \|Is a (attribute)\|	205564003 \|Congenital pigmentary skin anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9102391023) - 763368004 -> 724839001 (116680003) View
116680003 \|Is a (attribute)\|	724839001 \|Genetic disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9224402025) - 763368004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9224404029) - 763368004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	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
724839001 View
724839001	Genetic disorder of skin pigmentation (disorder)	Genetic disorder of skin pigmentation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
205564003 View
205564003	Congenital pigmentary skin anomalies (disorder)	Dị tật sắc tố da bẩm sinh	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 (e2703f6f-6b79-53be-9a24-7c7fc155e015) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.8	TRUE	ALWAYS L81.8 \| 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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