dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 40488004

Production

add

Language with ID “2ee0ed0f-7d78-58f7-9103-a46e8652034d” doesn’t exist. Perhaps it was deleted?

Component

40488004

The component that hold information about this concept.

Fully Specified Name (FSN)

Fanconi syndrome (disorder)

Shortest Term

Fanconi 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

Fanconi syndrome (disorder)

SCTID: 40488004, Primitive, Active

40488004|Fanconi syndrome (disorder)|

en Fanconi syndrome (disorder)
en Fanconi syndrome

Expression

40488004 |Fanconi syndrome (disorder)|
 <<< 95568003 |Renal tubular disorder (disorder)| + 
16784003 |Amino acid transport disorder (disorder)| + 
106000008 |Metabolic renal disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 58471003 |Renal tubule structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
777141012 - Fanconi syndrome (disorder) (en) View
777141012	en	Fully specified name (core metadata concept)	Fanconi syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
67513013 - Fanconi syndrome (en) View
67513013	en	Synonym (core metadata concept)	Fanconi syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
67514019 - Fanconi syndrome, NOS (en) View
67514019	en	Synonym (core metadata concept)	Fanconi syndrome, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15058015024) - 40488004 -> 106000008 (116680003) View
116680003 \|Is a (attribute)\|	106000008 \|Metabolic renal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (773245022) - 40488004 -> 58471003 (363698007) View
363698007 \|Finding site (attribute)\|	58471003 \|Renal tubule structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (214041020) - 40488004 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (773243026) - 40488004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (773242020) - 40488004 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (773244021) - 40488004 -> 50235001 (363698007) View
363698007 \|Finding site (attribute)\|	50235001 \|Structure of interstitial tissue of kidney (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1674676020) - 40488004 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (214039024) - 40488004 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (214038027) - 40488004 -> 95568003 (116680003) View
116680003 \|Is a (attribute)\|	95568003 \|Renal tubular disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (214040021) - 40488004 -> 16784003 (116680003) View
116680003 \|Is a (attribute)\|	16784003 \|Amino acid transport disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
106000008 View
106000008	Metabolic renal disease (disorder)	Metabolic renal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95568003 View
95568003	Renal tubular disorder (disorder)	Rối loạn ống thận	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
16784003 View
16784003	Amino acid transport disorder (disorder)	Amino acid transport disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1269271003 View
1269271003	Atypical fanconi syndrome, neonatal hyperinsulinism syndrome (disorder)	Atypical fanconi syndrome, neonatal hyperinsulinism syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236467001 View
236467001	Acquired fanconi syndrome (disorder)	Acquired fanconi syndrome	900000000000073002 \|Sufficiently defined by necessary conditions 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 (beaee464-8e65-5d01-a6a9-5e9b0aaa2b6d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.0	TRUE	ALWAYS E72.0	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 40488004

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches