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Terminology chevron_right Concepts chevron_right 82852009

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Sex-linked hereditary disorder (disorder)

Shortest Term

Sex-linked hereditary disorder

Definition Status

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

Summary

Sex-linked hereditary disorder (disorder)

SCTID: 82852009, Primitive, Active

82852009|Sex-linked hereditary disorder (disorder)|

Expression

82852009 |Sex-linked hereditary disorder (disorder)|
 <<< 32895009 |Hereditary disease (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
137435012 - Sex-linked hereditary disorder (en) View
137435012	en	Synonym (core metadata concept)	Sex-linked hereditary disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
824362013 - Sex-linked hereditary disorder (disorder) (en) View
824362013	en	Fully specified name (core metadata concept)	Sex-linked hereditary disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
137436013 - Sex-linked hereditary disorder, NOS (en) View
137436013	en	Synonym (core metadata concept)	Sex-linked hereditary disorder, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (282737024) - 82852009 -> 32895009 (116680003) View
116680003 \|Is a (attribute)\|	32895009 \|Hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
32895009 View
32895009	Hereditary disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
232013002 View
232013002	Macular retinoschisis (disorder)	Macular retinoschisis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
80908008 View
80908008	Ornithine carbamoyltransferase deficiency (disorder)	Octd	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
81771002 View
81771002	Opitz-frias syndrome (disorder)	G syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128430005 View
128430005	X-linked hereditary disease (disorder)	X-linked hereditary disease	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 (ac8bfcee-ea05-5074-ae0f-5bd994f9402f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

Descriptions