dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 44553005

Production

add

Component

44553005

The component that hold information about this concept.

Fully Specified Name (FSN)

Dubin-johnson syndrome (disorder)

Shortest Term

Spinz-nelson 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

Dubin-johnson syndrome (disorder)

SCTID: 44553005, Primitive, Active

44553005|Dubin-johnson syndrome (disorder)|

vi Hội chứng dubin-johnson
en Sprinz nelson syndrome
en Black liver-jaundice syndrome
en Chronic idiopathic jaundice with pigmented liver
en Icterus-hepatic pigmentation syndrome
en Dubin-johnson syndrome (disorder)
en Djs - dubin-johnson syndrome
en Dubin-johnson syndrome
en Dubin-sprinz syndrome
en Hyperbilirubinaemia ii
en Hyperbilirubinemia ii

Expression

44553005 |Dubin-johnson syndrome (disorder)|
 <<< 9326001 |Conjugated hyperbilirubinemia (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
5655007 |Inherited disorder of bilirubin metabolism (disorder)| + 
89166001 |Congenital anomaly of liver (disorder)| + 
414032001 |Disorder of pigmentation (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
300331000 |Lesion of liver (disorder)| + 
235903001 |Metabolic and genetic disorder affecting the liver (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 51083003 |Structure showing abnormal deposition of pigment (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 10200004 |Liver 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
458081000003114 - hội chứng Dubin-Johnson (vi) View
458081000003114	vi	Synonym (core metadata concept)	hội chứng Dubin-Johnson	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
74314011 - Spinz-Nelson syndrome (en) View
74314011	en	Synonym (core metadata concept)	Spinz-Nelson syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
3791287016 - Sprinz Nelson syndrome (en) View
3791287016	en	Synonym (core metadata concept)	Sprinz Nelson syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
74311015 - Black liver-jaundice syndrome (en) View
74311015	en	Synonym (core metadata concept)	Black liver-jaundice syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
74312010 - Chronic idiopathic jaundice with pigmented liver (en) View
74312010	en	Synonym (core metadata concept)	Chronic idiopathic jaundice with pigmented liver	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
74315012 - Icterus-hepatic pigmentation syndrome (en) View
74315012	en	Synonym (core metadata concept)	Icterus-hepatic pigmentation syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
781695016 - Dubin-Johnson syndrome (disorder) (en) View
781695016	en	Fully specified name (core metadata concept)	Dubin-Johnson syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
493925014 - DJS - Dubin-Johnson syndrome (en) View
493925014	en	Synonym (core metadata concept)	DJS - Dubin-Johnson syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
74310019 - Dubin-Johnson syndrome (en) View
74310019	en	Synonym (core metadata concept)	Dubin-Johnson syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
74313017 - Dubin-Sprinz syndrome (en) View
74313017	en	Synonym (core metadata concept)	Dubin-Sprinz syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
493924013 - Hyperbilirubinaemia II (en) View
493924013	en	Synonym (core metadata concept)	Hyperbilirubinaemia II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
493923019 - Hyperbilirubinemia II (en) View
493923019	en	Synonym (core metadata concept)	Hyperbilirubinemia II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3001088024) - 44553005 -> 362975008 (116680003) View
116680003 \|Is a (attribute)\|	362975008 \|Degenerative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13068956020) - 44553005 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (783379026) - 44553005 -> 51083003 (116676008) View
116676008 \|Associated morphology (attribute)\|	51083003 \|Structure showing abnormal deposition of pigment (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10527540024) - 44553005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12086541022) - 44553005 -> 300331000 (116680003) View
116680003 \|Is a (attribute)\|	300331000 \|Lesion of liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12086542026) - 44553005 -> 235903001 (116680003) View
116680003 \|Is a (attribute)\|	235903001 \|Metabolic and genetic disorder affecting the liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12086543020) - 44553005 -> 51083003 (116676008) View
116676008 \|Associated morphology (attribute)\|	51083003 \|Structure showing abnormal deposition of pigment (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3466992023) - 44553005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980470027) - 44553005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980471028) - 44553005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980472024) - 44553005 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10527541023) - 44553005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527542027) - 44553005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (783377029) - 44553005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3179211020) - 44553005 -> 363024001 (116680003) View
116680003 \|Is a (attribute)\|	363024001 \|Congenital anomaly of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3181357028) - 44553005 -> 363026004 (116680003) View
116680003 \|Is a (attribute)\|	363026004 \|Congenital anomaly of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (783376022) - 44553005 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1767533023) - 44553005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3310830024) - 44553005 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1675538026) - 44553005 -> 55056006 (116680003) View
116680003 \|Is a (attribute)\|	55056006 \|Hepatic porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2770839027) - 44553005 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2692318029) - 44553005 -> 414032001 (116680003) View
116680003 \|Is a (attribute)\|	414032001 \|Disorder of pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (783375021) - 44553005 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (783378023) - 44553005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2030525020) - 44553005 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1767534028) - 44553005 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (220556026) - 44553005 -> 14783006 (116680003) View
116680003 \|Is a (attribute)\|	14783006 \|Hyperbilirubinemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (220558025) - 44553005 -> 27503000 (116680003) View
116680003 \|Is a (attribute)\|	27503000 \|Gilbert's syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1675537020) - 44553005 -> 5655007 (116680003) View
116680003 \|Is a (attribute)\|	5655007 \|Inherited disorder of bilirubin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1675539023) - 44553005 -> 89166001 (116680003) View
116680003 \|Is a (attribute)\|	89166001 \|Congenital anomaly of liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (220557024) - 44553005 -> 9326001 (116680003) View
116680003 \|Is a (attribute)\|	9326001 \|Conjugated hyperbilirubinemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (220559022) - 44553005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (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
300331000 View
300331000	Lesion of liver (disorder)	Tổn thương gan	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
414032001 View
414032001	Disorder of pigmentation (disorder)	Disorder of pigmentation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
5655007 View
5655007	Inherited disorder of bilirubin metabolism (disorder)	Inherited disorder of bilirubin metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
9326001 View
9326001	Conjugated hyperbilirubinemia (disorder)	Conjugated hyperbilirubinemia	900000000000074008 \|Necessary but not sufficient concept 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
89166001 View
89166001	Congenital anomaly of liver (disorder)	Dị tật gan bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
235903001 View
235903001	Metabolic and genetic disorder affecting the liver (disorder)	Rối loạn chuyển hóa và di truyền ảnh hưởng đến gan	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 (328cee61-6286-53d4-a974-ffdfce891de3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.6	TRUE	ALWAYS E80.6	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 44553005

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches