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371313002: Congenital cerebellar cortical atrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1196610013 Congenital cerebellar cortical atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1209985010 Congenital cerebellar cortical atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229023011 Familial convulsions AND/OR ataxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1196610013 Congenital cerebellar cortical atrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1196610013 Congenital cerebellar cortical atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1209985010 Congenital cerebellar cortical atrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1209985010 Congenital cerebellar cortical atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229023011 Familial convulsions AND/OR ataxia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
85681000077114 atrophie corticale cérébelleuse congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
85681000077114 atrophie corticale cérébelleuse congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital cerebellar cortical atrophy (disorder) Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar cortical atrophy (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar cortical atrophy (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Is a Cerebellar disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Is a Dysgenesis of the cerebellum false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Is a Degenerative disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Is a Cerebellar disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Finding site Cerebellar cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Finding site Cerebellar cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cerebellar cortical atrophy (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Is a Cerebellar disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cerebellar cortical atrophy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar cortical atrophy (disorder) Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar cortical atrophy (disorder) Finding site Cerebellar cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital cerebellar cortical atrophy (disorder) Is a Cerebellar degeneration true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial febrile convulsions Is a False Congenital cerebellar cortical atrophy (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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