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Terminology chevron_right Concepts chevron_right 238092004

Production

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Component

238092004

The component that hold information about this concept.

Fully Specified Name (FSN)

Fish-eye disease (disorder)

Shortest Term

Fish-eye 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

Fish-eye disease (disorder)

SCTID: 238092004, Primitive, Active

238092004|Fish-eye disease (disorder)|

en Partial lcat deficiency
en Partial lcat (lecithin-cholesterol acyltransferase) deficiency
en Fish-eye disease
en Fish-eye disease (disorder)
en Fed - fish-eye disease

Expression

238092004 |Fish-eye disease (disorder)|
 <<< 238091006 |Lecithin cholesterol acyltransferase deficiency (disorder)| + 
128289001 |Chronic metabolic disorder (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 28036006 |High density lipoprotein cholesterol measurement (procedure)| }
        { 116676008 |Associated morphology (attribute)| = 128305008 |Abnormally opaque structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 28726007 |Corneal structure (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5173419017 - Partial LCAT deficiency (en) View
5173419017	en	Synonym (core metadata concept)	Partial LCAT deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
5173418013 - Partial LCAT (lecithin-cholesterol acyltransferase) deficiency (en) View
5173418013	en	Synonym (core metadata concept)	Partial LCAT (lecithin-cholesterol acyltransferase) deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
356907019 - Fish-eye disease (en) View
356907019	en	Synonym (core metadata concept)	Fish-eye disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626926016 - Fish-eye disease (disorder) (en) View
626926016	en	Fully specified name (core metadata concept)	Fish-eye disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
356908012 - FED - Fish-eye disease (en) View
356908012	en	Synonym (core metadata concept)	FED - Fish-eye disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (527214024) - 238092004 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15516128026) - 238092004 -> 28726007 (363698007) View
363698007 \|Finding site (attribute)\|	28726007 \|Corneal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516129023) - 238092004 -> 128305008 (116676008) View
116676008 \|Associated morphology (attribute)\|	128305008 \|Abnormally opaque structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516143029) - 238092004 -> 128289001 (116680003) View
116680003 \|Is a (attribute)\|	128289001 \|Chronic metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516144024) - 238092004 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516145020) - 238092004 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516146021) - 238092004 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516147028) - 238092004 -> 28036006 (363714003) View
363714003 \|Interprets (attribute)\|	28036006 \|High density lipoprotein cholesterol measurement (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15516148022) - 238092004 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2713159027) - 238092004 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2254101023) - 238092004 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (527213029) - 238092004 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (527215020) - 238092004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53754029) - 238092004 -> 238091006 (116680003) View
116680003 \|Is a (attribute)\|	238091006 \|Lecithin cholesterol acyltransferase deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128289001 View
128289001	Chronic metabolic disorder (disorder)	Chronic metabolic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
238091006 View
238091006	Lecithin cholesterol acyltransferase deficiency (disorder)	Lcat deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363343008 View
363343008	Hereditary disorder of the visual system (disorder)	Hereditary disorder of the visual 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 (e4d2b628-2bd6-598d-a106-e65d2783f7dc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E78.6	TRUE	ALWAYS E78.6 \| 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)\|

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