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Terminology chevron_right Concepts chevron_right 783620009

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Component

783620009

The component that hold information about this concept.

Fully Specified Name (FSN)

Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)

Shortest Term

Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis

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

Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)

SCTID: 783620009, Primitive, Active

783620009|Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)|

vi Giảm phosphat máu chiếm ưu thế với bệnh sỏi thận và/hoặc loãng xương
en Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis
en Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
en Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)

Expression

783620009 |Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)|
 <<< 237890006 |Autosomal dominant hypophosphatemic bone disease (disorder)| + 
367591000119105 |Hereditary nephropathy (disorder)| + 
106000008 |Metabolic renal disease (disorder)| + 
49698005 |Urinary complication (disorder)| + 
95568003 |Renal tubular disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39365008 |Osteoid tissue (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 128416000 |Impaired mineralization (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 272673000 |Bone structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 58471003 |Renal tubule structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 42752001 |Due to (attribute)| = 236470002 |Specific renal tubule transport defect (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4181000269110 - giảm phosphat máu chiếm ưu thế với bệnh sỏi thận và/hoặc loãng xương (vi) View
4181000269110	vi	Synonym (core metadata concept)	giảm phosphat máu chiếm ưu thế với bệnh sỏi thận và/hoặc loãng xương	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3759537018 - Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis (en) View
3759537018	en	Synonym (core metadata concept)	Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3759533019 - Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (en) View
3759533019	en	Synonym (core metadata concept)	Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3759536010 - Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder) (en) View
3759536010	en	Fully specified name (core metadata concept)	Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15058029020) - 783620009 -> 106000008 (116680003) View
116680003 \|Is a (attribute)\|	106000008 \|Metabolic renal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14011372023) - 783620009 -> 49698005 (116680003) View
116680003 \|Is a (attribute)\|	49698005 \|Urinary complication (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11575537027) - 783620009 -> 236470002 (42752001) View
42752001 \|Due to (attribute)\|	236470002 \|Specific renal tubule transport defect (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11575538021) - 783620009 -> 58471003 (363698007) View
363698007 \|Finding site (attribute)\|	58471003 \|Renal tubule structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094668028) - 783620009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094669020) - 783620009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094670021) - 783620009 -> 128416000 (116676008) View
116676008 \|Associated morphology (attribute)\|	128416000 \|Impaired mineralization (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094671020) - 783620009 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12877518020) - 783620009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877521022) - 783620009 -> 128416000 (116676008) View
116676008 \|Associated morphology (attribute)\|	128416000 \|Impaired mineralization (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877522026) - 783620009 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877523020) - 783620009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877524025) - 783620009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877525029) - 783620009 -> 58471003 (363698007) View
363698007 \|Finding site (attribute)\|	58471003 \|Renal tubule structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877526028) - 783620009 -> 236470002 (42752001) View
42752001 \|Due to (attribute)\|	236470002 \|Specific renal tubule transport defect (disorder)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312817021) - 783620009 -> 39365008 (363698007) View
363698007 \|Finding site (attribute)\|	39365008 \|Osteoid tissue (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312818027) - 783620009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312819024) - 783620009 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312820029) - 783620009 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312821025) - 783620009 -> 95568003 (116680003) View
116680003 \|Is a (attribute)\|	95568003 \|Renal tubular disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312823027) - 783620009 -> 237890006 (116680003) View
116680003 \|Is a (attribute)\|	237890006 \|Autosomal dominant hypophosphatemic bone disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11312824022) - 783620009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	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
49698005 View
49698005	Urinary complication (disorder)	Urinary complication	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
237890006 View
237890006	Autosomal dominant hypophosphatemic bone disease (disorder)	Hypercalciuric rickets	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
95568003 View
95568003	Renal tubular disorder (disorder)	Rối loạn ống thận	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 (86dd918b-211d-5eaa-b754-7c85a12489c8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N25.8	TRUE	ALWAYS N25.8 \| 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)\|
ExtendedMap object (ec29c86d-b99b-5acc-aaad-6ef4b85505e9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.3	TRUE	ALWAYS E83.3 \| 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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