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Terminology chevron_right Concepts chevron_right 61860000

Production

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Component

61860000

The component that hold information about this concept.

Fully Specified Name (FSN)

Porphyria cutanea tarda (disorder)

Shortest Term

Pct

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

Porphyria cutanea tarda (disorder)

SCTID: 61860000, Primitive, Active

61860000|Porphyria cutanea tarda (disorder)|

vi Rối loạn chuyển hóa porpyrin biểu hiện da muộn
en Chp - cutaneous hepatic porphyria
en Pct - porphyria cutanea tarda
en Cutaneous hepatic porphyria
en Porphyria cutanea tarda
en Porphyria cutanea tarda (disorder)
en Porphyria cutanea tarda symptomatica
en Porphyria, hepatocutaneous type
en Symptomatic porphyria
en Urocoproporphyria

Expression

61860000 |Porphyria cutanea tarda (disorder)|
 <<< 55056006 |Hepatic porphyria (disorder)| + 
276262000 |Uroporphyrinogen decarboxylase deficiency (disorder)| + 
95320005 |Disorder of skin (disorder)| : 
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
444901000003112 - rối loạn chuyển hóa porpyrin biểu hiện da muộn (vi) View
444901000003112	vi	Synonym (core metadata concept)	rối loạn chuyển hóa porpyrin biểu hiện da muộn	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
5244080019 - CHP - cutaneous hepatic porphyria (en) View
5244080019	en	Synonym (core metadata concept)	CHP - cutaneous hepatic porphyria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
499145012 - CHP - Cutaneous hepatic porphyria (en) View
499145012	en	Synonym (core metadata concept)	CHP - Cutaneous hepatic porphyria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
102823011 - PCT (en) View
102823011	en	Synonym (core metadata concept)	PCT	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
5244083017 - PCT - porphyria cutanea tarda (en) View
5244083017	en	Synonym (core metadata concept)	PCT - porphyria cutanea tarda	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
499144011 - PCT - Porphyria cutanea tarda (en) View
499144011	en	Synonym (core metadata concept)	PCT - Porphyria cutanea tarda	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
102827012 - UROD deficiency (en) View
102827012	en	Synonym (core metadata concept)	UROD deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
102822018 - Cutaneous hepatic porphyria (en) View
102822018	en	Synonym (core metadata concept)	Cutaneous hepatic porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
102819015 - Porphyria cutanea tarda (en) View
102819015	en	Synonym (core metadata concept)	Porphyria cutanea tarda	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
800968016 - Porphyria cutanea tarda (disorder) (en) View
800968016	en	Fully specified name (core metadata concept)	Porphyria cutanea tarda (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
102824017 - Porphyria cutanea tarda symptomatica (en) View
102824017	en	Synonym (core metadata concept)	Porphyria cutanea tarda symptomatica	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
102825016 - Porphyria, hepatocutaneous type (en) View
102825016	en	Synonym (core metadata concept)	Porphyria, hepatocutaneous type	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
102821013 - Symptomatic porphyria (en) View
102821013	en	Synonym (core metadata concept)	Symptomatic porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
102826015 - Urocoproporphyria (en) View
102826015	en	Synonym (core metadata concept)	Urocoproporphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
102820014 - Porphyria cutanea tarda, NOS (en) View
102820014	en	Synonym (core metadata concept)	Porphyria cutanea tarda, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (828095028) - 61860000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (828097020) - 61860000 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4601544024) - 61860000 -> 280128006 (116680003) View
116680003 \|Is a (attribute)\|	280128006 \|Disorder of soft tissue of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2549269027) - 61860000 -> 280128006 (116680003) View
116680003 \|Is a (attribute)\|	280128006 \|Disorder of soft tissue of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (248696026) - 61860000 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (828096027) - 61860000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (248697024) - 61860000 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1679100025) - 61860000 -> 95320005 (116680003) View
116680003 \|Is a (attribute)\|	95320005 \|Disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (248698025) - 61860000 -> 55056006 (116680003) View
116680003 \|Is a (attribute)\|	55056006 \|Hepatic porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (248699022) - 61860000 -> 276262000 (116680003) View
116680003 \|Is a (attribute)\|	276262000 \|Uroporphyrinogen decarboxylase deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
55056006 View
55056006	Hepatic porphyria (disorder)	Hepatic porphyria	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95320005 View
95320005	Disorder of skin (disorder)	Dermatosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
276262000 View
276262000	Uroporphyrinogen decarboxylase deficiency (disorder)	Uroporphyrinogen decarboxylase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1155910005 View
1155910005	Acquired porphyria cutanea tarda (disorder)	Acquired porphyria cutanea tarda	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
402479002 View
402479002	Sporadic porphyria cutanea tarda (disorder)	Acquired hepatic porphyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
59229005 View
59229005	Familial porphyria cutanea tarda (disorder)	Pct, type ii	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
111386004 View
111386004	Homozygous porphyria cutanea tarda (disorder)	Hepatoerythropoietic porphyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (e1587885-c06f-5ee7-9310-7b4b29a66f62) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.1	TRUE	ALWAYS E80.1	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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