dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 205564003

Production

add

Component

205564003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital pigmentary skin anomalies (disorder)

Shortest Term

Dị tật sắc tố da bẩm sinh

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

Congenital pigmentary skin anomalies (disorder)

SCTID: 205564003, Defined, Active

205564003|Congenital pigmentary skin anomalies (disorder)|

vi Dị tật sắc tố da bẩm sinh
en Congenital pigmentary anomaly of skin
en Congenital pigmentary skin anomalies
en Congenital pigmentary skin anomalies (disorder)

Expression

205564003 |Congenital pigmentary skin anomalies (disorder)|
 === 199879009 |Congenital anomaly of skin (disorder)| + 
46690002 |Disorder of skin pigmentation (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
573781000003111 - dị tật sắc tố da bẩm sinh (vi) View
573781000003111	vi	Synonym (core metadata concept)	dị tật sắc tố da bẩm sinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2475672012 - Congenital pigmentary anomaly of skin (en) View
2475672012	en	Synonym (core metadata concept)	Congenital pigmentary anomaly of skin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
315243010 - Congenital pigmentary skin anomalies (en) View
315243010	en	Synonym (core metadata concept)	Congenital pigmentary skin anomalies	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
590950015 - Congenital pigmentary skin anomalies (disorder) (en) View
590950015	en	Fully specified name (core metadata concept)	Congenital pigmentary skin anomalies (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4971837026) - 205564003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4971838020) - 205564003 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4995793020) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10528196022) - 205564003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2791968025) - 205564003 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3081494021) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6040175021) - 205564003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6040176022) - 205564003 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6040177029) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (971745025) - 205564003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1075930021) - 205564003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3081493026) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2958549020) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2958550020) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2893174022) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2893175023) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2791969022) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2791970023) - 205564003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971739022) - 205564003 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2234908024) - 205564003 -> 238907001 (116680003) View
116680003 \|Is a (attribute)\|	238907001 \|Site-specific disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2773972025) - 205564003 -> 46690002 (116680003) View
116680003 \|Is a (attribute)\|	46690002 \|Disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (331036024) - 205564003 -> 60447007 (116680003) View
116680003 \|Is a (attribute)\|	60447007 \|Congenital anomaly of tongue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (331037026) - 205564003 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (331038020) - 205564003 -> 13213009 (116680003) View
116680003 \|Is a (attribute)\|	13213009 \|Congenital heart disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971740024) - 205564003 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971741023) - 205564003 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971744026) - 205564003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971746029) - 205564003 -> 62834003 (363698007) View
363698007 \|Finding site (attribute)\|	62834003 \|Upper gastrointestinal tract structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971747022) - 205564003 -> 80891009 (363698007) View
363698007 \|Finding site (attribute)\|	80891009 \|Heart structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971748028) - 205564003 -> 21974007 (363698007) View
363698007 \|Finding site (attribute)\|	21974007 \|Tongue structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1075931020) - 205564003 -> 118970008 (363698007) View
363698007 \|Finding site (attribute)\|	118970008 \|Cardiovascular system subdivision (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1694582021) - 205564003 -> 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
46690002 View
46690002	Disorder of skin pigmentation (disorder)	Dyschromia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
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
897554004 View
897554004	Dermal melanocytic hamartoma (disorder)	Dermal melanocytic hamartoma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
239079007 View
239079007	Inherited cutaneous hyperpigmentation (disorder)	Inherited cutaneous hyperpigmentation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
771262009 View
771262009	Pseudoleprechaunism syndrome patterson type (disorder)	Patterson syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
763368004 View
763368004	Familial progressive hyperpigmentation and hypopigmentation of skin (disorder)	Familial progressive hyper and hypopigmentation	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
765195000 View
765195000	Familial generalized lentiginosis (disorder)	Familial lentigines profusa	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
766881008 View
766881008	Carney complex, trismus, pseudocamptodactyly syndrome (disorder)	Carney complex variant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724091002 View
724091002	Neuroectodermal melanolysosomal disease (disorder)	Elejalde disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
726029005 View
726029005	Mccune albright syndrome (disorder)	Mccune albright syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
733469003 View
733469003	Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome (disorder)	Westerhof beemer cormane syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1953005 View
1953005	Congenital deficiency of pigment of skin (disorder)	Congenital deficiency of pigment of skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
51089004 View
51089004	Birthmark (disorder)	Birthmark	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 (8240e464-3a5b-5070-b9b0-23c513021bec) 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)\|

Terminology chevron_right Concepts chevron_right 205564003

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches