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Terminology chevron_right Concepts chevron_right 197601003

Production

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Component

197601003

The component that hold information about this concept.

Fully Specified Name (FSN)

Finnish congenital nephrotic syndrome (disorder)

Shortest Term

Congenital finnish nephrosis

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

Finnish congenital nephrotic syndrome (disorder)

SCTID: 197601003, Primitive, Active

197601003|Finnish congenital nephrotic syndrome (disorder)|

en Finnish congenital nephrotic syndrome (disorder)
en Cnf - finnish congenital nephrotic syndrome
en Congenital finnish nephrosis
en Finnish congenital nephrotic syndrome

Expression

197601003 |Finnish congenital nephrotic syndrome (disorder)|
 <<< 48796009 |Congenital nephrotic syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68288006 |Glomerulus structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 26758005 |Albumin measurement (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 57378007 |Measurement of protein in urine (procedure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
581998015 - Finnish congenital nephrotic syndrome (disorder) (en) View
581998015	en	Fully specified name (core metadata concept)	Finnish congenital nephrotic syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
303841014 - CNF - Finnish congenital nephrotic syndrome (en) View
303841014	en	Synonym (core metadata concept)	CNF - Finnish congenital nephrotic syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
303842019 - Congenital Finnish nephrosis (en) View
303842019	en	Synonym (core metadata concept)	Congenital Finnish nephrosis	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
303840010 - Finnish congenital nephrotic syndrome (en) View
303840010	en	Synonym (core metadata concept)	Finnish congenital nephrotic syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3351460027) - 197601003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989510026) - 197601003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5043432027) - 197601003 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10548811022) - 197601003 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10548812026) - 197601003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10548813020) - 197601003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102475021) - 197601003 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102476022) - 197601003 -> 26758005 (363714003) View
363714003 \|Interprets (attribute)\|	26758005 \|Albumin measurement (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102477029) - 197601003 -> 57378007 (363714003) View
363714003 \|Interprets (attribute)\|	57378007 \|Measurement of protein in urine (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102478023) - 197601003 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (465340020) - 197601003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (465339023) - 197601003 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (465342028) - 197601003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3351461028) - 197601003 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (465341024) - 197601003 -> 122489005 (363698007) View
363698007 \|Finding site (attribute)\|	122489005 \|Urinary system structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (465343022) - 197601003 -> 211384000 (260908002) View
260908002 \|Course (attribute)\|	211384000 \|Multiple superficial injuries of lower leg (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (21319027) - 197601003 -> 48796009 (116680003) View
116680003 \|Is a (attribute)\|	48796009 \|Congenital nephrotic syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
48796009 View
48796009	Congenital nephrotic syndrome (disorder)	Familial nephrotic syndrome	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 (dd57a188-9015-5948-8a6a-a9a621365a20) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N04.8	TRUE	ALWAYS N04.8 \| 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)\|

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