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9091417024
The component that hold information about this relationship.
763312008 |Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder)|
Identifies the source concept of the relationship version. That is the concept defined by this relationship. Set to the identifier of a concept.
85995004 |Autosomal recessive hereditary disorder (disorder)|
Identifies the concept that is the destination of the relationship version. That is the concept representing the value of the attribute represented by the typeId column. Set to the identifier of a concept. Note that the values that can be applied to particular attributes are formally defined by the SNOMED CT Machine Readable Concept Model.
0
Groups together relationship versions that are part of a logically associated relationshipGroup. All activeRelationship records with the same relationshipGroup number and sourceId are grouped in this way.
116680003 |Is a (attribute)|
Identifies the concept that represent the defining attribute (or relationship type) represented by this relationship version. That is the concept representing the value of the attribute represented by the typeId column. Set to the identifier of a concept. The concept identified must be either 116680003 | Is a| or a subtype of 410662002 | Concept model attribute| .
900000000000011006 |Inferred relationship (core metadata concept)|
A concept enumeration value that identifies the characteristic type of the relationship version (i.e. whether the relationship version is defining, qualifying, etc.) This field is set to a descendant of 900000000000449001
900000000000451002 |Existential restriction modifier (core metadata concept)|
A concept enumeration value that identifies the type of Description Logic (DL) restriction (some, all, etc.). Set to a child of 900000000000450001
True
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