dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 279082008

Production

add

Component

279082008

The component that hold information about this concept.

Fully Specified Name (FSN)

Acromesomelic dysplasia group (disorder)

Shortest Term

Acromesomelic dwarfism

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

Acromesomelic dysplasia group (disorder)

SCTID: 279082008, Primitive, Active

279082008|Acromesomelic dysplasia group (disorder)|

en Acromesomelic dwarfism
en Acromesomelic dysplasia
en Acromesomelic dysplasia group
en Acromesomelic dysplasia group (disorder)
en Acromesomelic dysplasia syndrome

Expression

279082008 |Acromesomelic dysplasia group (disorder)|
 <<< 105986008 |Congenital skeletal dysplasia (disorder)| + 
8447006 |Congenital anomaly of skeletal bone (disorder)| + 
879976004 |Lesion of bone (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (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)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
416206016 - Acromesomelic dwarfism (en) View
416206016	en	Synonym (core metadata concept)	Acromesomelic dwarfism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
416207013 - Acromesomelic dysplasia (en) View
416207013	en	Synonym (core metadata concept)	Acromesomelic dysplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
416205017 - Acromesomelic dysplasia group (en) View
416205017	en	Synonym (core metadata concept)	Acromesomelic dysplasia group	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
672321019 - Acromesomelic dysplasia group (disorder) (en) View
672321019	en	Fully specified name (core metadata concept)	Acromesomelic dysplasia group (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
416204018 - Acromesomelic dysplasia syndrome (en) View
416204018	en	Synonym (core metadata concept)	Acromesomelic dysplasia syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16413161025) - 279082008 -> 879976004 (116680003) View
116680003 \|Is a (attribute)\|	879976004 \|Lesion of bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (606148027) - 279082008 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3321243022) - 279082008 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286287028) - 279082008 -> 8447006 (116680003) View
116680003 \|Is a (attribute)\|	8447006 \|Congenital anomaly of skeletal bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (606145029) - 279082008 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4976859025) - 279082008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4987202024) - 279082008 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5023149024) - 279082008 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6131302024) - 279082008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527138022) - 279082008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (606146028) - 279082008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3321244027) - 279082008 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1740001025) - 279082008 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (606149024) - 279082008 -> 281242000 (363698007) View
363698007 \|Finding site (attribute)\|	281242000 \|Musculoskeletal structure of limb (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1661625020) - 279082008 -> 128605003 (116680003) View
116680003 \|Is a (attribute)\|	128605003 \|Disorder of extremity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (606147021) - 279082008 -> 113192009 (363698007) View
363698007 \|Finding site (attribute)\|	113192009 \|Skeletal system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (97502027) - 279082008 -> 105986008 (116680003) View
116680003 \|Is a (attribute)\|	105986008 \|Congenital skeletal dysplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
879976004 View
879976004	Lesion of bone (disorder)	Lesion of bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
8447006 View
8447006	Congenital anomaly of skeletal bone (disorder)	Congenital skeletal anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
105986008 View
105986008	Congenital skeletal dysplasia (disorder)	Osteodysplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1187277001 View
1187277001	Short stature, brachydactyly, obesity, global developmental delay syndrome (disorder)	Short stature, brachydactyly, obesity, global developmental delay syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724147004 View
724147004	8q13 microdeletion syndrome (disorder)	Monosomy 8q13	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
718559000 View
718559000	Acromesomelic dysplasia maroteaux type (disorder)	Acromesomelic dysplasia maroteaux type	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
720416007 View
720416007	Acrocapitofemoral dysplasia (disorder)	Acrocapitofemoral dysplasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
389167007 View
389167007	Acromesomelic dysplasia hunter-thompson type (disorder)	Hunter-thompson dysplasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
389168002 View
389168002	Brachydactyly syndrome type b (disorder)	Brachydactyly syndrome type b	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
389169005 View
389169005	Brachydactyly syndrome type c (disorder)	Brachydactyly syndrome type c	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
28557005 View
28557005	Geleophysic dysplasia (disorder)	Geleophysic dysplasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
58833000 View
58833000	Pseudohypoparathyroidism type i a (disorder)	Pseudohypoparathyroidism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63711009 View
63711009	Brachydactyly syndrome type e (disorder)	Brachydactyly syndrome type e	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
66758006 View
66758006	Acrodysostosis (disorder)	Acrodysostosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
77542002 View
77542002	Grebe syndrome (disorder)	Grebe syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
254090007 View
254090007	Acromicric dysplasia (disorder)	Acromicric dysplasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
254093009 View
254093009	Cranioectodermal dysplasia (disorder)	Sensenbrenner's syndrome	900000000000074008 \|Necessary but not sufficient concept 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 (53de0c56-d0e0-55d6-893e-7a8567d99111) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.9	TRUE	ALWAYS Q78.9	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 (5e7983ef-79ea-5216-8736-aaf05c21401d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q73.8	TRUE	ALWAYS Q73.8	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 279082008

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches