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Terminology chevron_right Concepts chevron_right 725905005

Production

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Component

725905005

The component that hold information about this concept.

Fully Specified Name (FSN)

Infundibulopelvic stenosis multicystic kidney syndrome (disorder)

Shortest Term

Infundibulopelvic dysgenesis

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

Infundibulopelvic stenosis multicystic kidney syndrome (disorder)

SCTID: 725905005, Primitive, Active

725905005|Infundibulopelvic stenosis multicystic kidney syndrome (disorder)|

vi Hội chứng thận đa nang hẹp đài bể thận
en Infundibulopelvic dysgenesis
en Infundibulopelvic stenosis multicystic kidney syndrome
en Infundibulopelvic stenosis multicystic kidney syndrome (disorder)

Expression

725905005 |Infundibulopelvic stenosis multicystic kidney syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
44513007 |Congenital anomaly of the kidney (disorder)| + 
118642009 |Congenital anomaly of the urinary tract proper (disorder)| + 
367591000119105 |Hereditary nephropathy (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
896984006 |Structural abnormality of renal collecting system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 279371005 |Renal collecting system structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
7771000269119 - hội chứng thận đa nang hẹp đài bể thận (vi) View
7771000269119	vi	Synonym (core metadata concept)	hội chứng thận đa nang hẹp đài bể thận	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3446284016 - Infundibulopelvic dysgenesis (en) View
3446284016	en	Synonym (core metadata concept)	Infundibulopelvic dysgenesis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3446283010 - Infundibulopelvic stenosis multicystic kidney syndrome (en) View
3446283010	en	Synonym (core metadata concept)	Infundibulopelvic stenosis multicystic kidney syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3446282017 - Infundibulopelvic stenosis multicystic kidney syndrome (disorder) (en) View
3446282017	en	Fully specified name (core metadata concept)	Infundibulopelvic stenosis multicystic kidney syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16381906023) - 725905005 -> 896984006 (116680003) View
116680003 \|Is a (attribute)\|	896984006 \|Structural abnormality of renal collecting system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069501020) - 725905005 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913240025) - 725905005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10514832028) - 725905005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514833022) - 725905005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913236023) - 725905005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913237025) - 725905005 -> 44513007 (116680003) View
116680003 \|Is a (attribute)\|	44513007 \|Congenital anomaly of the kidney (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913238024) - 725905005 -> 118642009 (116680003) View
116680003 \|Is a (attribute)\|	118642009 \|Congenital anomaly of the urinary tract proper (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913239027) - 725905005 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913241026) - 725905005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913242022) - 725905005 -> 279371005 (363698007) View
363698007 \|Finding site (attribute)\|	279371005 \|Renal collecting system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
896984006 View
896984006	Structural abnormality of renal collecting system (disorder)	Abnormal renal collecting system morphology	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
367591000119105 View
367591000119105	Hereditary nephropathy (disorder)	Hereditary nephropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
44513007 View
44513007	Congenital anomaly of the kidney (disorder)	Congenital anomaly of kidney	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
118642009 View
118642009	Congenital anomaly of the urinary tract proper (disorder)	Congenital anomaly of the urinary tract	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 (e99ec463-1c8c-589f-a734-59ebfd339f17) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q63.8	TRUE	ALWAYS Q63.8 \| 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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