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Terminology chevron_right Concepts chevron_right 36517007

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Component

36517007

The component that hold information about this concept.

Fully Specified Name (FSN)

Polyostotic fibrous dysplasia of bone (disorder)

Shortest Term

Albright 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

Polyostotic fibrous dysplasia of bone (disorder)

SCTID: 36517007, Primitive, Active

36517007|Polyostotic fibrous dysplasia of bone (disorder)|

en Osteitis fibrosa disseminata
en Polyostotic fibrous dysplasia
en Polyostotic fibrous dysplasia of bone
en Polyostotic fibrous dysplasia of bone (disorder)
en Albright's disease of bone
en Albright syndrome
en Pfd - polyostotic fibrous dysplasia
en Pofd - polyostotic fibrous dysplasia

Expression

36517007 |Polyostotic fibrous dysplasia of bone (disorder)|
 <<< 10623005 |Fibrous dysplasia of bone (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 789439000 |Fibrous dysplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 272673000 |Bone structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
486481017 - Albright-McCune-Sternberg syndrome (en) View
486481017	en	Synonym (core metadata concept)	Albright-McCune-Sternberg syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
486480016 - Fibrous dysplasia with pigmentary skin changes and precocious puberty (en) View
486480016	en	Synonym (core metadata concept)	Fibrous dysplasia with pigmentary skin changes and precocious puberty	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
486474012 - MAS - McCune-Albright syndrome (en) View
486474012	en	Synonym (core metadata concept)	MAS - McCune-Albright syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
486475013 - McCune-Albright syndrome (en) View
486475013	en	Synonym (core metadata concept)	McCune-Albright syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
60954012 - Osteitis fibrosa disseminata (en) View
60954012	en	Synonym (core metadata concept)	Osteitis fibrosa disseminata	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
486476014 - Polyostotic fibrous dysplasia (en) View
486476014	en	Synonym (core metadata concept)	Polyostotic fibrous dysplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
60952011 - Polyostotic fibrous dysplasia of bone (en) View
60952011	en	Synonym (core metadata concept)	Polyostotic fibrous dysplasia of bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
768278018 - Polyostotic fibrous dysplasia of bone (disorder) (en) View
768278018	en	Fully specified name (core metadata concept)	Polyostotic fibrous dysplasia of bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
486477017 - Albright's disease of bone (en) View
486477017	en	Synonym (core metadata concept)	Albright's disease of bone	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
486482012 - Albright syndrome (en) View
486482012	en	Synonym (core metadata concept)	Albright syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
486478010 - PFD - Polyostotic fibrous dysplasia (en) View
486478010	en	Synonym (core metadata concept)	PFD - Polyostotic fibrous dysplasia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
486479019 - POFD - Polyostotic fibrous dysplasia (en) View
486479019	en	Synonym (core metadata concept)	POFD - Polyostotic fibrous dysplasia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
60953018 - Polyostotic fibrous dysplasia of bone, NOS (en) View
60953018	en	Synonym (core metadata concept)	Polyostotic fibrous dysplasia of bone, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10515597024) - 36517007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13068946021) - 36517007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (207383022) - 36517007 -> 254140006 (116680003) View
116680003 \|Is a (attribute)\|	254140006 \|Disorganized development of cartilaginous and fibrous components of the skeleton (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (509887028) - 36517007 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4799101026) - 36517007 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4983352025) - 36517007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10515598025) - 36517007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11227424021) - 36517007 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286265021) - 36517007 -> 771314001 (363698007) View
363698007 \|Finding site (attribute)\|	771314001 \|Cartilage structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286266022) - 36517007 -> 77881008 (116680003) View
116680003 \|Is a (attribute)\|	77881008 \|Osteochondropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286267029) - 36517007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12074335022) - 36517007 -> 789439000 (116676008) View
116676008 \|Associated morphology (attribute)\|	789439000 \|Fibrous dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3432576029) - 36517007 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763070029) - 36517007 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4992533026) - 36517007 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5023664020) - 36517007 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763069025) - 36517007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3432575025) - 36517007 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4799102022) - 36517007 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4799103028) - 36517007 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1764839022) - 36517007 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763066021) - 36517007 -> 113192009 (363698007) View
363698007 \|Finding site (attribute)\|	113192009 \|Skeletal system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (207384027) - 36517007 -> 10623005 (116680003) View
116680003 \|Is a (attribute)\|	10623005 \|Fibrous dysplasia of bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
10623005 View
10623005	Fibrous dysplasia of bone (disorder)	Osteitis fibrosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
699346009 View
699346009	Hereditary cancer-predisposing syndrome (disorder)	Hereditary neoplastic syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal 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 (a91d5769-405c-5b4b-aec0-67d012ae8a69) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.1	TRUE	ALWAYS Q78.1	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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