dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 721977007

Production

add

Component

721977007

The component that hold information about this concept.

Fully Specified Name (FSN)

Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome (disorder)

Shortest Term

Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis 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

Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome (disorder)

SCTID: 721977007, Primitive, Active

721977007|Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome (disorder)|

vi Xơ phổi, suy giảm miễn dịch, hội chứng rối loạn phát triển tuyến sinh dục 46, xx
en Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome
en Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome (disorder)

Expression

721977007 |Lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome (disorder)|
 <<< 51615001 |Fibrosis of lung (disorder)| + 
95198001 |Pure gonadal dysgenesis 46,xx (disorder)| + 
362993009 |Autosomal recessive severe combined immunodeficiency disease (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
363290007 |Reproductive system hereditary disorder (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
1335927007 |T-cell negative b-cell positive severe combined immunodeficiency (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 60877009 |Hormone secretion, function (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 112674009 |Fibrosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39607008 |Lung structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 304043001 |Ovarian endocrine structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 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
489121000003112 - xơ phổi, suy giảm miễn dịch, hội chứng rối loạn phát triển tuyến sinh dục 46, XX (vi) View
489121000003112	vi	Synonym (core metadata concept)	xơ phổi, suy giảm miễn dịch, hội chứng rối loạn phát triển tuyến sinh dục 46, XX	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3330002017 - Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (en) View
3330002017	en	Synonym (core metadata concept)	Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3330001012 - Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder) (en) View
3330001012	en	Fully specified name (core metadata concept)	Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10520317021) - 721977007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10520319024) - 721977007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10520320029) - 721977007 -> 47147007 (116680003) View
116680003 \|Is a (attribute)\|	47147007 \|Congenital anomaly of lung (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16024152020) - 721977007 -> 1335927007 (116680003) View
116680003 \|Is a (attribute)\|	1335927007 \|T-cell negative b-cell positive severe combined immunodeficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069343025) - 721977007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11169869027) - 721977007 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762780025) - 721977007 -> 112674009 (116676008) View
116676008 \|Associated morphology (attribute)\|	112674009 \|Fibrosis (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6762782022) - 721977007 -> 39607008 (363698007) View
363698007 \|Finding site (attribute)\|	39607008 \|Lung structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6762783028) - 721977007 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6762784023) - 721977007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6762785024) - 721977007 -> 304043001 (363698007) View
363698007 \|Finding site (attribute)\|	304043001 \|Ovarian endocrine structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6767598020) - 721977007 -> 304043001 (363698007) View
363698007 \|Finding site (attribute)\|	304043001 \|Ovarian endocrine structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10520318027) - 721977007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10538417029) - 721977007 -> 112674009 (116676008) View
116676008 \|Associated morphology (attribute)\|	112674009 \|Fibrosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10538418023) - 721977007 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10538419026) - 721977007 -> 39607008 (363698007) View
363698007 \|Finding site (attribute)\|	39607008 \|Lung structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762779028) - 721977007 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7602809028) - 721977007 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7602810022) - 721977007 -> 60877009 (363714003) View
363714003 \|Interprets (attribute)\|	60877009 \|Hormone secretion, function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762774022) - 721977007 -> 51615001 (116680003) View
116680003 \|Is a (attribute)\|	51615001 \|Fibrosis of lung (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762775023) - 721977007 -> 95198001 (116680003) View
116680003 \|Is a (attribute)\|	95198001 \|Pure gonadal dysgenesis 46,xx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762776024) - 721977007 -> 362993009 (116680003) View
116680003 \|Is a (attribute)\|	362993009 \|Autosomal recessive severe combined immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762777026) - 721977007 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762778020) - 721977007 -> 363290007 (116680003) View
116680003 \|Is a (attribute)\|	363290007 \|Reproductive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6762781026) - 721977007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1335927007 View
1335927007	T-cell negative b-cell positive severe combined immunodeficiency (disorder)	T-cell negative b-cell positive severe combined immunodeficiency	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
362993009 View
362993009	Autosomal recessive severe combined immunodeficiency disease (disorder)	Autosomal recessive scid	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
51615001 View
51615001	Fibrosis of lung (disorder)	Xơ phổi	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95198001 View
95198001	Pure gonadal dysgenesis 46,xx (disorder)	Pure gonadal dysgenesis 46,xx	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
363290007 View
363290007	Reproductive system hereditary disorder (disorder)	Reproductive 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 (084a42d3-4163-5178-85af-fdaabc3f0357) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q99.1	TRUE	ALWAYS Q99.1	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)\|
ExtendedMap object (5223c1b9-d368-5b96-8d80-96e86836058f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D82.8	TRUE	ALWAYS D82.8 \| 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)\|
ExtendedMap object (5d51399e-ec5b-59de-85c0-dbadd370bd5e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q99.1	TRUE	ALWAYS Q99.1	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)\|
ExtendedMap object (bd33f085-5312-5e38-a110-918f610c939a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	J84.1	TRUE	ALWAYS J84.1	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)\|
ExtendedMap object (fd796032-3c9f-5bf9-ba94-6b32cbe46561) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	J84.1	TRUE	ALWAYS J84.1	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)\|

Terminology chevron_right Concepts chevron_right 721977007

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches