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Terminology chevron_right Concepts chevron_right 774211005

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Component

774211005

The component that hold information about this concept.

Fully Specified Name (FSN)

Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)

Shortest Term

Sam syndrome

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

Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)

SCTID: 774211005, Primitive, Active

774211005|Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)|

en Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome
en Sam syndrome
en Severe dermatitis, multiple allergies, metabolic wasting syndrome
en Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)

Expression

774211005 |Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)|
 <<< 442459007 |Combined immunodeficiency disease (disorder)| + 
36138009 |Congenital immunodeficiency disease (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363138005 |Hereditary disorder of immune system (disorder)| + 
363185004 |Hereditary disorder of the integument (disorder)| + 
199879009 |Congenital anomaly of skin (disorder)| + 
399992009 |Erythroderma (disorder)| + 
131136006 |Immunoglobulin above reference range (finding)| + 
58921009 |Diffuse dermatitis (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 103626005 |Diffuse inflammation (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)| }
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 41960005 |Immunoglobulin e measurement (procedure)| }
        { 116676008 |Associated morphology (attribute)| = 70819003 |Erythema (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3728379019 - Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome (en) View
3728379019	en	Synonym (core metadata concept)	Congenital erythroderma, hypotrichosis, recurrent infections, multiple food allergies syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3728380016 - SAM syndrome (en) View
3728380016	en	Synonym (core metadata concept)	SAM syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3728377017 - Severe dermatitis, multiple allergies, metabolic wasting syndrome (en) View
3728377017	en	Synonym (core metadata concept)	Severe dermatitis, multiple allergies, metabolic wasting syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3728378010 - Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder) (en) View
3728378010	en	Fully specified name (core metadata concept)	Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13070031027) - 774211005 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11170431020) - 774211005 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11355001023) - 774211005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11355002027) - 774211005 -> 70819003 (116676008) View
116676008 \|Associated morphology (attribute)\|	70819003 \|Erythema (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11355003021) - 774211005 -> 58921009 (116680003) View
116680003 \|Is a (attribute)\|	58921009 \|Diffuse dermatitis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718270026) - 774211005 -> 442459007 (116680003) View
116680003 \|Is a (attribute)\|	442459007 \|Combined immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718271027) - 774211005 -> 36138009 (116680003) View
116680003 \|Is a (attribute)\|	36138009 \|Congenital immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718272023) - 774211005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718273029) - 774211005 -> 363138005 (116680003) View
116680003 \|Is a (attribute)\|	363138005 \|Hereditary disorder of immune system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718274024) - 774211005 -> 103626005 (116676008) View
116676008 \|Associated morphology (attribute)\|	103626005 \|Diffuse inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718275020) - 774211005 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718276021) - 774211005 -> 199879009 (116680003) View
116680003 \|Is a (attribute)\|	199879009 \|Congenital anomaly of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718277028) - 774211005 -> 41960005 (363714003) View
363714003 \|Interprets (attribute)\|	41960005 \|Immunoglobulin e measurement (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718278022) - 774211005 -> 399992009 (116680003) View
116680003 \|Is a (attribute)\|	399992009 \|Erythroderma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718279025) - 774211005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718280027) - 774211005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718281028) - 774211005 -> 131136006 (116680003) View
116680003 \|Is a (attribute)\|	131136006 \|Immunoglobulin above reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718282024) - 774211005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10718283025) - 774211005 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
399992009 View
399992009	Erythroderma (disorder)	Erythroderma	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
131136006 View
131136006	Immunoglobulin above reference range (finding)	Increased immunoglobulin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
442459007 View
442459007	Combined immunodeficiency disease (disorder)	Combined immunodeficiency disease	900000000000074008 \|Necessary but not sufficient concept 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
36138009 View
36138009	Congenital immunodeficiency disease (disorder)	Congenital immunodeficiency disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
58921009 View
58921009	Diffuse dermatitis (disorder)	Diffuse dermatitis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363138005 View
363138005	Hereditary disorder of immune system (disorder)	Hereditary disorder of immune system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (3fc7affe-52ec-5c09-8166-846537d97a79) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8 \| 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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