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Terminology chevron_right Concepts chevron_right 37495007

Production

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Component

37495007

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial adrenocortical hypoplasia (disorder)

Shortest Term

Familial addison disease

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

Familial adrenocortical hypoplasia (disorder)

SCTID: 37495007, Primitive, Active

37495007|Familial adrenocortical hypoplasia (disorder)|

en Familial adrenocortical hypoplasia
en Familial adrenocortical hypoplasia (disorder)
en Familial cytomegalic adrenocortical hypoplasia
en Familial addison disease

Expression

37495007 |Familial adrenocortical hypoplasia (disorder)|
 <<< 363104002 |Hereditary disorder of endocrine system (disorder)| + 
111941005 |Familial disease (disorder)| + 
93235007 |Congenital hypoplasia of adrenal gland (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68594002 |Adrenal cortex 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
62535012 - Familial adrenocortical hypoplasia (en) View
62535012	en	Synonym (core metadata concept)	Familial adrenocortical hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
769367015 - Familial adrenocortical hypoplasia (disorder) (en) View
769367015	en	Fully specified name (core metadata concept)	Familial adrenocortical hypoplasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
62537016 - Familial cytomegalic adrenocortical hypoplasia (en) View
62537016	en	Synonym (core metadata concept)	Familial cytomegalic adrenocortical hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
62536013 - Familial Addison disease (en) View
62536013	en	Synonym (core metadata concept)	Familial Addison disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13068947028) - 37495007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10515851028) - 37495007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (765603027) - 37495007 -> 68594002 (363698007) View
363698007 \|Finding site (attribute)\|	68594002 \|Adrenal cortex structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (765604022) - 37495007 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2002287021) - 37495007 -> 386584007 (116680003) View
116680003 \|Is a (attribute)\|	386584007 \|Adrenal cortical hypofunction (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112096027) - 37495007 -> 93235007 (116680003) View
116680003 \|Is a (attribute)\|	93235007 \|Congenital hypoplasia of adrenal gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7112097020) - 37495007 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7112098026) - 37495007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7112099023) - 37495007 -> 68594002 (363698007) View
363698007 \|Finding site (attribute)\|	68594002 \|Adrenal cortex structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (208945029) - 37495007 -> 68588005 (116680003) View
116680003 \|Is a (attribute)\|	68588005 \|Adrenal cortical hypofunction (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (208946028) - 37495007 -> 363290007 (116680003) View
116680003 \|Is a (attribute)\|	363290007 \|Reproductive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (765605023) - 37495007 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (208947021) - 37495007 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (208948027) - 37495007 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (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
93235007 View
93235007	Congenital hypoplasia of adrenal gland (disorder)	Congenital adrenal hypoplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
111941005 View
111941005	Familial disease (disorder)	Familial disease	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 (f1299a73-7125-5c9d-8a7e-142058a3485e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E27.1	TRUE	ALWAYS E27.1	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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