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722965000: Parkinsonism due to heredodegenerative disorder (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334045015 Parkinsonism due to heredodegenerative disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334046019 Parkinsonism due to heredodegenerative disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334045015 Parkinsonism due to heredodegenerative disorder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334045015 Parkinsonism due to heredodegenerative disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334046019 Parkinsonism due to heredodegenerative disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334046019 Parkinsonism due to heredodegenerative disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6445711000241114 parkinsonisme dû à un trouble hérédodégénératif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6445721000241119 syndrome parkinsonien dû à un trouble hérédodégénératif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6445711000241114 parkinsonisme dû à un trouble hérédodégénératif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6445721000241119 syndrome parkinsonien dû à un trouble hérédodégénératif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Parkinsonism due to heredodegenerative disorder (disorder) Due to Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept) 2
Parkinsonism due to heredodegenerative disorder (disorder) Is a Secondary parkinsonism true Inferred relationship Existential restriction modifier (core metadata concept)
Parkinsonism due to heredodegenerative disorder (disorder) Finding site Basal ganglion structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Parkinsonism due to heredodegenerative disorder (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Parkinsonism due to heredodegenerative disorder (disorder) Has interpretation Slow true Inferred relationship Existential restriction modifier (core metadata concept) 4
Parkinsonism due to heredodegenerative disorder (disorder) Is a Central nervous system complication true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Parkinsonian pyramidal syndrome (disorder) Is a True Parkinsonism due to heredodegenerative disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Parkinsonism due to hereditary spastic paraplegia (disorder) Is a True Parkinsonism due to heredodegenerative disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

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