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Terminology chevron_right Concepts chevron_right 237606005

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Component

237606005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary benign acanthosis nigricans with insulin resistance (disorder)

Shortest Term

Insulin-resistant acanthosis nigricans type a

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

Hereditary benign acanthosis nigricans with insulin resistance (disorder)

SCTID: 237606005, Defined, Active

237606005|Hereditary benign acanthosis nigricans with insulin resistance (disorder)|

en Hereditary benign acanthosis nigricans with insulin resistance
en Hereditary benign acanthosis nigricans with insulin resistance (disorder)
en Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans
en Insulin-resistant acanthosis nigricans type a

Expression

237606005 |Hereditary benign acanthosis nigricans with insulin resistance (disorder)|
 === 10680005 |Insulin receptor defect (disorder)| + 
238634000 |Benign acanthosis nigricans (disorder)| + 
86042009 |Congenital melanosis (disorder)| + 
239079007 |Inherited cutaneous hyperpigmentation (disorder)| + 
403804008 |Hereditary hypermelanosis (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 26996000 |Hyperkeratosis (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)| }
        { 116676008 |Associated morphology (attribute)| = 48010006 |Melanosis (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)| }
        { 363698007 |Finding site (attribute)| = 113331007 |Structure of endocrine system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
356091012 - Hereditary benign acanthosis nigricans with insulin resistance (en) View
356091012	en	Synonym (core metadata concept)	Hereditary benign acanthosis nigricans with insulin resistance	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626360017 - Hereditary benign acanthosis nigricans with insulin resistance (disorder) (en) View
626360017	en	Fully specified name (core metadata concept)	Hereditary benign acanthosis nigricans with insulin resistance (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
356093010 - Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans (en) View
356093010	en	Synonym (core metadata concept)	Insulin receptor defect with insulin-resistant diabetes mellitus and acanthosis nigricans	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
356092017 - Insulin-resistant acanthosis nigricans type A (en) View
356092017	en	Synonym (core metadata concept)	Insulin-resistant acanthosis nigricans type A	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12876720029) - 237606005 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9337489021) - 237606005 -> 205564003 (116680003) View
116680003 \|Is a (attribute)\|	205564003 \|Congenital pigmentary skin anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9337497025) - 237606005 -> 724839001 (116680003) View
116680003 \|Is a (attribute)\|	724839001 \|Genetic disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11265572024) - 237606005 -> 239001006 (116680003) View
116680003 \|Is a (attribute)\|	239001006 \|Genodermatosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12072890023) - 237606005 -> 239079007 (116680003) View
116680003 \|Is a (attribute)\|	239079007 \|Inherited cutaneous hyperpigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12209807023) - 237606005 -> 403804008 (116680003) View
116680003 \|Is a (attribute)\|	403804008 \|Hereditary hypermelanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526229025) - 237606005 -> 113331007 (363698007) View
363698007 \|Finding site (attribute)\|	113331007 \|Structure of endocrine system (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9337490028) - 237606005 -> 44138005 (363714003) View
363714003 \|Interprets (attribute)\|	44138005 \|Keratinization, function (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9337491029) - 237606005 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9337493026) - 237606005 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9337494021) - 237606005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9337496023) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9343566029) - 237606005 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9349231022) - 237606005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10523548029) - 237606005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10523549021) - 237606005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2254059025) - 237606005 -> 69707008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	69707008 \|Abnormal keratinization (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3376130025) - 237606005 -> 23620008 (116676008) View
116676008 \|Associated morphology (attribute)\|	23620008 \|Acanthosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5980372026) - 237606005 -> 52988006 (116676008) View
116676008 \|Associated morphology (attribute)\|	52988006 \|Lesion (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7341125028) - 237606005 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9337498024) - 237606005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9337499027) - 237606005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9349230023) - 237606005 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9502688020) - 237606005 -> 86042009 (116680003) View
116680003 \|Is a (attribute)\|	86042009 \|Congenital melanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1656669025) - 237606005 -> 281867008 (116680003) View
116680003 \|Is a (attribute)\|	281867008 \|Multisystem disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2445878029) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526228022) - 237606005 -> 23620008 (116676008) View
116676008 \|Associated morphology (attribute)\|	23620008 \|Acanthosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3376131026) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2254060024) - 237606005 -> 31390008 (116676008) View
116676008 \|Associated morphology (attribute)\|	31390008 \|Epithelial hyperplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2515492025) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526227028) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2212390021) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1729673027) - 237606005 -> 1806006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1806006 \|Eruption (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2195241023) - 237606005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53145022) - 237606005 -> 312565003 (116680003) View
116680003 \|Is a (attribute)\|	312565003 \|Multisystem disorder a-b (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53146023) - 237606005 -> 10680005 (116680003) View
116680003 \|Is a (attribute)\|	10680005 \|Insulin receptor defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (53147025) - 237606005 -> 238634000 (116680003) View
116680003 \|Is a (attribute)\|	238634000 \|Benign acanthosis nigricans (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
403804008 View
403804008	Hereditary hypermelanosis (disorder)	Hereditary hypermelanosis	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
86042009 View
86042009	Congenital melanosis (disorder)	Congenital melanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
10680005 View
10680005	Insulin receptor defect (disorder)	Insulin receptor defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
238634000 View
238634000	Benign acanthosis nigricans (disorder)	Pseudoacanthosis nigricans	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	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 (017f44e0-74dc-5e95-86e9-de947193c3bf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.8	TRUE	ALWAYS E88.8	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)\|
ExtendedMap object (4059b55d-a90e-5b2d-82f5-7ab6355695bf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E16.8	TRUE	ALWAYS E16.8	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)\|
ExtendedMap object (eb8dd1fb-a361-5a88-84ef-88667858843f) 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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