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Terminology chevron_right Concepts chevron_right 45414006

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Component

45414006

The component that hold information about this concept.

Fully Specified Name (FSN)

Glucocorticoid deficiency with achalasia (disorder)

Shortest Term

Allgrove 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

Glucocorticoid deficiency with achalasia (disorder)

SCTID: 45414006, Primitive, Active

45414006|Glucocorticoid deficiency with achalasia (disorder)|

en Achalasia-addisonian syndrome
en Alacrimia-achalasia-addisonianism
en Glucocorticoid deficiency with achalasia
en Glucocorticoid deficiency with achalasia (disorder)
en Allgrove syndrome
en Triple a syndrome

Expression

45414006 |Glucocorticoid deficiency with achalasia (disorder)|
 <<< 85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
700283004 |Congenital achalasia of esophagus (disorder)| + 
1156181008 |Adrenocorticotropic hormone resistance syndrome (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 398598008 |Motility (observable entity)| }
        { 363698007 |Finding site (attribute)| = 25271004 |Cardioesophageal junction structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 68594002 |Adrenal cortex structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 69748006 |Thyroid structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
75714016 - Achalasia-addisonian syndrome (en) View
75714016	en	Synonym (core metadata concept)	Achalasia-addisonian syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
75717011 - Alacrimia-achalasia-addisonianism (en) View
75717011	en	Synonym (core metadata concept)	Alacrimia-achalasia-addisonianism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
75713010 - Glucocorticoid deficiency with achalasia (en) View
75713010	en	Synonym (core metadata concept)	Glucocorticoid deficiency with achalasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
782651012 - Glucocorticoid deficiency with achalasia (disorder) (en) View
782651012	en	Fully specified name (core metadata concept)	Glucocorticoid deficiency with achalasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
75715015 - Allgrove syndrome (en) View
75715015	en	Synonym (core metadata concept)	Allgrove syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
75716019 - Triple A syndrome (en) View
75716019	en	Synonym (core metadata concept)	Triple A syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (1675720026) - 45414006 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2030854020) - 45414006 -> 386584007 (116680003) View
116680003 \|Is a (attribute)\|	386584007 \|Adrenal cortical hypofunction (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13805446029) - 45414006 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13805447022) - 45414006 -> 1156181008 (116680003) View
116680003 \|Is a (attribute)\|	1156181008 \|Adrenocorticotropic hormone resistance syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13805448028) - 45414006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7119485027) - 45414006 -> 32849002 (363698007) View
363698007 \|Finding site (attribute)\|	32849002 \|Esophageal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (785359021) - 45414006 -> 68594002 (363698007) View
363698007 \|Finding site (attribute)\|	68594002 \|Adrenal cortex structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1675717023) - 45414006 -> 45564002 (116680003) View
116680003 \|Is a (attribute)\|	45564002 \|Achalasia of esophagus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1767803022) - 45414006 -> 25271004 (363698007) View
363698007 \|Finding site (attribute)\|	25271004 \|Cardioesophageal junction structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1767804027) - 45414006 -> 48531003 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	48531003 \|Achalasia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112105020) - 45414006 -> 700283004 (116680003) View
116680003 \|Is a (attribute)\|	700283004 \|Congenital achalasia of esophagus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7112108022) - 45414006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7115690026) - 45414006 -> 25271004 (363698007) View
363698007 \|Finding site (attribute)\|	25271004 \|Cardioesophageal junction structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7117835021) - 45414006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7119486026) - 45414006 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7119487024) - 45414006 -> 398598008 (363714003) View
363714003 \|Interprets (attribute)\|	398598008 \|Motility (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7119488025) - 45414006 -> 68594002 (363698007) View
363698007 \|Finding site (attribute)\|	68594002 \|Adrenal cortex structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (221974022) - 45414006 -> 68588005 (116680003) View
116680003 \|Is a (attribute)\|	68588005 \|Adrenal cortical hypofunction (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (785360027) - 45414006 -> 48531003 (363714003) View
363714003 \|Interprets (attribute)\|	48531003 \|Achalasia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (785361028) - 45414006 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1675718029) - 45414006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1675719021) - 45414006 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1156181008 View
1156181008	Adrenocorticotropic hormone resistance syndrome (disorder)	Adrenocorticotropin resistance syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
700283004 View
700283004	Congenital achalasia of esophagus (disorder)	Congenital achalasia of esophagus	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
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	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 (c296ff6a-a2d6-5162-a396-22a5424b010c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K22.0	TRUE	ALWAYS K22.0	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 (fa814b1c-a6dc-579d-aaf7-50605449bd9f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E27.4	TRUE	ALWAYS E27.4	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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