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Terminology chevron_right Concepts chevron_right 7425008

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Component

7425008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary coproporphyria (disorder)

Shortest Term

Cpo deficiency

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Hereditary coproporphyria (disorder)

SCTID: 7425008, Defined, Active

7425008|Hereditary coproporphyria (disorder)|

vi Rối loạn chuyển hóa coproporphyrin di truyền
en Coproporphyrinogen oxidase deficiency
en Hereditary coproporphyria
en Hereditary coproporphyria (disorder)
en Berger-goldberg syndrome
en Cpo - coproporphyrinogen oxidase deficiency
en Cpo deficiency
en Cpro deficiency
en Hcp - hereditary coproporphyria
en Porphyria hepatica ii

Expression

7425008 |Hereditary coproporphyria (disorder)|
 === 190915002 |Coproporphyria (disorder)| + 
55056006 |Hepatic porphyria (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
454541000003115 - rối loạn chuyển hóa coproporphyrin di truyền (vi) View
454541000003115	vi	Synonym (core metadata concept)	rối loạn chuyển hóa coproporphyrin di truyền	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
502648018 - Watson's syndrome (en) View
502648018	en	Synonym (core metadata concept)	Watson's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
13243010 - Watson syndrome (en) View
13243010	en	Synonym (core metadata concept)	Watson syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
502647011 - Coproporphyrinogen oxidase deficiency (en) View
502647011	en	Synonym (core metadata concept)	Coproporphyrinogen oxidase deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
13238015 - Hereditary coproporphyria (en) View
13238015	en	Synonym (core metadata concept)	Hereditary coproporphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
814729016 - Hereditary coproporphyria (disorder) (en) View
814729016	en	Fully specified name (core metadata concept)	Hereditary coproporphyria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
13239011 - Berger-Goldberg syndrome (en) View
13239011	en	Synonym (core metadata concept)	Berger-Goldberg syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
502649014 - CPO - Coproporphyrinogen oxidase deficiency (en) View
502649014	en	Synonym (core metadata concept)	CPO - Coproporphyrinogen oxidase deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
13240013 - CPO deficiency (en) View
13240013	en	Synonym (core metadata concept)	CPO deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
13241012 - CPRO deficiency (en) View
13241012	en	Synonym (core metadata concept)	CPRO deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
502646019 - HCP - Hereditary coproporphyria (en) View
502646019	en	Synonym (core metadata concept)	HCP - Hereditary coproporphyria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
13242017 - Porphyria hepatica II (en) View
13242017	en	Synonym (core metadata concept)	Porphyria hepatica II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2867025029) - 7425008 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1681762022) - 7425008 -> 281867008 (116680003) View
116680003 \|Is a (attribute)\|	281867008 \|Multisystem disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7340979025) - 7425008 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1681763028) - 7425008 -> 29094004 (116680003) View
116680003 \|Is a (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2842973023) - 7425008 -> 190915002 (116680003) View
116680003 \|Is a (attribute)\|	190915002 \|Coproporphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2842974028) - 7425008 -> 55056006 (116680003) View
116680003 \|Is a (attribute)\|	55056006 \|Hepatic porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (268774023) - 7425008 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268776020) - 7425008 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268778021) - 7425008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268781027) - 7425008 -> 23853001 (116680003) View
116680003 \|Is a (attribute)\|	23853001 \|Disorder of the central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859259020) - 7425008 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859260026) - 7425008 -> 39057004 (363698007) View
363698007 \|Finding site (attribute)\|	39057004 \|Pulmonary valve structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859261027) - 7425008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859262023) - 7425008 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1681761026) - 7425008 -> 76267008 (116680003) View
116680003 \|Is a (attribute)\|	76267008 \|Pulmonary valve disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2230997027) - 7425008 -> 238907001 (116680003) View
116680003 \|Is a (attribute)\|	238907001 \|Site-specific disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2550665028) - 7425008 -> 280129003 (116680003) View
116680003 \|Is a (attribute)\|	280129003 \|Disorder of soft tissue of thoracic cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2550666027) - 7425008 -> 13213009 (116680003) View
116680003 \|Is a (attribute)\|	13213009 \|Congenital heart disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268780026) - 7425008 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1681760025) - 7425008 -> 95320005 (116680003) View
116680003 \|Is a (attribute)\|	95320005 \|Disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268773028) - 7425008 -> 312557001 (116680003) View
116680003 \|Is a (attribute)\|	312557001 \|Multisystem disorder w-x (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268775024) - 7425008 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268777027) - 7425008 -> 56265001 (116680003) View
116680003 \|Is a (attribute)\|	56265001 \|Heart disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268779029) - 7425008 -> 86292002 (116680003) View
116680003 \|Is a (attribute)\|	86292002 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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
190915002 View
190915002	Coproporphyria (disorder)	Coproporphyria	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
61164006 View
61164006	Erythropoietic coproporphyria (disorder)	Erythropoietic coproporphyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
238056003 View
238056003	Homozygous hereditary coproporphyria (disorder)	Harderoporphyria	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 (6c9aa7bf-a1ed-5695-8a6b-1d036b4392ad) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	TRUE	ALWAYS E80.2	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)\|

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2867025029) - 7425008 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1681762022) - 7425008 -> 281867008 (116680003) View
116680003 \|Is a (attribute)\|	281867008 \|Multisystem disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7340979025) - 7425008 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1681763028) - 7425008 -> 29094004 (116680003) View
116680003 \|Is a (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2842973023) - 7425008 -> 190915002 (116680003) View
116680003 \|Is a (attribute)\|	190915002 \|Coproporphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2842974028) - 7425008 -> 55056006 (116680003) View
116680003 \|Is a (attribute)\|	55056006 \|Hepatic porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (268774023) - 7425008 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268776020) - 7425008 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268778021) - 7425008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268781027) - 7425008 -> 23853001 (116680003) View
116680003 \|Is a (attribute)\|	23853001 \|Disorder of the central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859259020) - 7425008 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859260026) - 7425008 -> 39057004 (363698007) View
363698007 \|Finding site (attribute)\|	39057004 \|Pulmonary valve structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859261027) - 7425008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (859262023) - 7425008 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1681761026) - 7425008 -> 76267008 (116680003) View
116680003 \|Is a (attribute)\|	76267008 \|Pulmonary valve disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2230997027) - 7425008 -> 238907001 (116680003) View
116680003 \|Is a (attribute)\|	238907001 \|Site-specific disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2550665028) - 7425008 -> 280129003 (116680003) View
116680003 \|Is a (attribute)\|	280129003 \|Disorder of soft tissue of thoracic cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2550666027) - 7425008 -> 13213009 (116680003) View
116680003 \|Is a (attribute)\|	13213009 \|Congenital heart disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268780026) - 7425008 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1681760025) - 7425008 -> 95320005 (116680003) View
116680003 \|Is a (attribute)\|	95320005 \|Disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268773028) - 7425008 -> 312557001 (116680003) View
116680003 \|Is a (attribute)\|	312557001 \|Multisystem disorder w-x (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268775024) - 7425008 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268777027) - 7425008 -> 56265001 (116680003) View
116680003 \|Is a (attribute)\|	56265001 \|Heart disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268779029) - 7425008 -> 86292002 (116680003) View
116680003 \|Is a (attribute)\|	86292002 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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