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Terminology chevron_right Concepts chevron_right 239079007

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Component

239079007

The component that hold information about this concept.

Fully Specified Name (FSN)

Inherited cutaneous hyperpigmentation (disorder)

Shortest Term

Inherited cutaneous hyperpigmentation

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

Inherited cutaneous hyperpigmentation (disorder)

SCTID: 239079007, Defined, Active

239079007|Inherited cutaneous hyperpigmentation (disorder)|

en Inherited cutaneous hyperpigmentation
en Inherited cutaneous hyperpigmentation (disorder)

Expression

239079007 |Inherited cutaneous hyperpigmentation (disorder)|
 === 239001006 |Genodermatosis (disorder)| + 
49765009 |Hyperpigmentation of skin (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)| = 4830009 |Hyperpigmentation (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
358290010 - Inherited cutaneous hyperpigmentation (en) View
358290010	en	Synonym (core metadata concept)	Inherited cutaneous hyperpigmentation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
628047011 - Inherited cutaneous hyperpigmentation (disorder) (en) View
628047011	en	Fully specified name (core metadata concept)	Inherited cutaneous hyperpigmentation (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15392715025) - 239079007 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069783024) - 239079007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11300744022) - 239079007 -> 724839001 (116680003) View
116680003 \|Is a (attribute)\|	724839001 \|Genetic disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (530625025) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (530627022) - 239079007 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3082126022) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032494024) - 239079007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032495020) - 239079007 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032496021) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9648348028) - 239079007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648350020) - 239079007 -> 205564003 (116680003) View
116680003 \|Is a (attribute)\|	205564003 \|Congenital pigmentary skin anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514834027) - 239079007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11105934025) - 239079007 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (530624026) - 239079007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1730799026) - 239079007 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3082125021) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2959428026) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2959429023) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2894098021) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2894099029) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2800538024) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2800539027) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (530626029) - 239079007 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2575495026) - 239079007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2716228027) - 239079007 -> 238907001 (116680003) View
116680003 \|Is a (attribute)\|	238907001 \|Site-specific disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (55187022) - 239079007 -> 239001006 (116680003) View
116680003 \|Is a (attribute)\|	239001006 \|Genodermatosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (55188028) - 239079007 -> 49765009 (116680003) View
116680003 \|Is a (attribute)\|	49765009 \|Hyperpigmentation of skin (disorder)\|	0	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
49765009 View
49765009	Hyperpigmentation of skin (disorder)	Tăng sắc tố da	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
239001006 View
239001006	Genodermatosis (disorder)	Genodermatosis	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
1177178005 View
1177178005	Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder)	Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
787408008 View
787408008	Osteopathia striata, pigmentary dermopathy, white forelock syndrome (disorder)	Whyte murphy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
771179007 View
771179007	Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome (disorder)	Char douglas dungan syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
771182002 View
771182002	Thumb deformity, alopecia, pigmentation anomaly syndrome (disorder)	Sparse hair, short stature, skin anomalies syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
205583005 View
205583005	Hereditary benign acanthosis nigricans (disorder)	Hereditary benign acanthosis nigricans	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
237606005 View
237606005	Hereditary benign acanthosis nigricans with insulin resistance (disorder)	Insulin-resistant acanthosis nigricans type a	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
723578001 View
723578001	Terminal osseous dysplasia and pigmentary defect syndrome (disorder)	Terminal osseous dysplasia and pigmentary defect syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239082002 View
239082002	Dyschromatosis universalis (disorder)	Melanism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239084001 View
239084001	Naegeli-franceschetti-jadassohn syndrome (disorder)	Naegeli's syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239085000 View
239085000	Symmetrical dyschromatosis of extremities (disorder)	Acropigmentation of dohi	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239088003 View
239088003	Dermatopathia pigmentosa reticularis (disorder)	Dermatopathia pigmentosa reticularis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239089006 View
239089006	Acromelanosis (disorder)	Acromelanosis	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 (2e91d40b-01fa-59ca-8b50-a6bdf6046c2d) 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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