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Terminology chevron_right Concepts chevron_right 707607008

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Component

707607008

The component that hold information about this concept.

Fully Specified Name (FSN)

Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)

Shortest Term

Amelogenesis imperfecta and gingival hyperplasia 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

Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)

SCTID: 707607008, Primitive, Active

707607008|Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)|

en Amelogenesis imperfecta and gingival hyperplasia syndrome
en Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)

Expression

707607008 |Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)|
 <<< 78494001 |Amelogenesis imperfecta (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
441798003 |Hyperplasia of gingiva (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 76197007 |Hyperplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113279002 |Gingival structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 76993005 |Enamel 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
3030784010 - Amelogenesis imperfecta and gingival hyperplasia syndrome (en) View
3030784010	en	Synonym (core metadata concept)	Amelogenesis imperfecta and gingival hyperplasia syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3030774014 - Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder) (en) View
3030774014	en	Fully specified name (core metadata concept)	Amelogenesis imperfecta and gingival hyperplasia syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5982645020) - 707607008 -> 128456003 (363698007) View
363698007 \|Finding site (attribute)\|	128456003 \|Structure of hard tissue of tooth (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11292281027) - 707607008 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5982643029) - 707607008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5982646021) - 707607008 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5982647028) - 707607008 -> 113279002 (363698007) View
363698007 \|Finding site (attribute)\|	113279002 \|Gingival structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10532480029) - 707607008 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532481025) - 707607008 -> 113279002 (363698007) View
363698007 \|Finding site (attribute)\|	113279002 \|Gingival structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532482021) - 707607008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532483027) - 707607008 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532484022) - 707607008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532485023) - 707607008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5982641027) - 707607008 -> 249410009 (116680003) View
116680003 \|Is a (attribute)\|	249410009 \|Gingivae finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5982639028) - 707607008 -> 78494001 (116680003) View
116680003 \|Is a (attribute)\|	78494001 \|Amelogenesis imperfecta (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5982640026) - 707607008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5982642023) - 707607008 -> 441798003 (116680003) View
116680003 \|Is a (attribute)\|	441798003 \|Hyperplasia of gingiva (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5982644024) - 707607008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
78494001 View
78494001	Amelogenesis imperfecta (disorder)	Amelogenesis imperfecta	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
441798003 View
441798003	Hyperplasia of gingiva (disorder)	Hyperplastic gingiva	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept 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 (f1b7fda5-6631-55e7-8385-b913bf62ae0b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K00.5	TRUE	ALWAYS K00.5	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 (f710fa74-5add-56da-adbb-b1d9bd5574d8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K06.1	TRUE	ALWAYS K06.1	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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