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Terminology chevron_right Concepts chevron_right 397340004

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)

Shortest Term

Aml with recurrent genetic abnormality

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)

SCTID: 397340004, Primitive, Inactive

397340004|Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)|

en Acute myeloid leukaemia with recurrent genetic abnormality
en Acute myeloid leukemia with recurrent genetic abnormality
en Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)
en Aml with recurrent genetic abnormality

Expression

397340004 |Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1773083010 - Acute myeloid leukaemia with recurrent genetic abnormality (en) View
1773083010	en	Synonym (core metadata concept)	Acute myeloid leukaemia with recurrent genetic abnormality	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1774369012 - Acute myeloid leukemia with recurrent genetic abnormality (en) View
1774369012	en	Synonym (core metadata concept)	Acute myeloid leukemia with recurrent genetic abnormality	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1765258017 - Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality) (en) View
1765258017	en	Fully specified name (core metadata concept)	Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1785800017 - AML with recurrent genetic abnormality (en) View
1785800017	en	Synonym (core metadata concept)	AML with recurrent genetic abnormality	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13898959027) - 397340004 -> 1162928000 (116680003) View
116680003 \|Is a (attribute)\|	1162928000 \|Acute myeloid leukemia (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2705956025) - 397340004 -> 413443009 (116680003) View
116680003 \|Is a (attribute)\|	413443009 \|Acute myeloid leukemia - category (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2242177025) - 397340004 -> 17788007 (116680003) View
116680003 \|Is a (attribute)\|	17788007 \|Acute myeloid leukemia, no icd-o subtype (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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

Descriptions