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Terminology chevron_right Concepts chevron_right 1197215004

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Component

1197215004

The component that hold information about this concept.

Fully Specified Name (FSN)

Microform holoprosencephaly (disorder)

Shortest Term

Holoprosencephaly-like

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

Microform holoprosencephaly (disorder)

SCTID: 1197215004, Primitive, Active

1197215004|Microform holoprosencephaly (disorder)|

en Holoprosencephaly-like
en Holoprosencephaly minor form
en Hpe (holoprosencephaly) minor form
en Microform holoprosencephaly
en Microform holoprosencephaly (disorder)

Expression

1197215004 |Microform holoprosencephaly (disorder)|
 <<< 30915001 |Holoprosencephaly sequence (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 69536005 |Head 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
4695465011 - Holoprosencephaly-like (en) View
4695465011	en	Synonym (core metadata concept)	Holoprosencephaly-like	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4695462014 - Holoprosencephaly minor form (en) View
4695462014	en	Synonym (core metadata concept)	Holoprosencephaly minor form	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4695463016 - HPE (holoprosencephaly) minor form (en) View
4695463016	en	Synonym (core metadata concept)	HPE (holoprosencephaly) minor form	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4695464010 - Microform holoprosencephaly (en) View
4695464010	en	Synonym (core metadata concept)	Microform holoprosencephaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4695466012 - Microform holoprosencephaly (disorder) (en) View
4695466012	en	Fully specified name (core metadata concept)	Microform holoprosencephaly (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15028072027) - 1197215004 -> 30915001 (116680003) View
116680003 \|Is a (attribute)\|	30915001 \|Holoprosencephaly sequence (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15028073021) - 1197215004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15028074026) - 1197215004 -> 69536005 (363698007) View
363698007 \|Finding site (attribute)\|	69536005 \|Head structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15028075025) - 1197215004 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15028076029) - 1197215004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
30915001 View
30915001	Holoprosencephaly sequence (disorder)	Arhinencephaly	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 (3178fb5e-0ca8-514a-a3d5-19cf895b0df8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.2	TRUE	ALWAYS Q04.2 \| 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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