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371313002: Congenital cerebellar cortical atrophy (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
1196610013 Congenital cerebellar cortical atrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1209985010 Congenital cerebellar cortical atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
1229023011 Familial convulsions AND/OR ataxia en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital cerebellar cortical atrophy Is a Degenerative disease of the central nervous system false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Congenital cerebellar cortical atrophy Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 2
Congenital cerebellar cortical atrophy Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Is a Cerebellar disorder false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Is a Dysgenesis of the cerebellum false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Is a Degenerative disorder false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Is a Cerebellar disorder false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Finding site Cerebellar cortex structure false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Associated morphology Congenital atrophy false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Finding site Cerebellar cortex structure false Inferred relationship Existential restriction modifier 1
Congenital cerebellar cortical atrophy Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Is a Cerebellar disorder false Inferred relationship Existential restriction modifier
Congenital cerebellar cortical atrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital cerebellar cortical atrophy Associated morphology Atrophy true Inferred relationship Existential restriction modifier 2
Congenital cerebellar cortical atrophy Finding site Cerebellar cortex structure true Inferred relationship Existential restriction modifier 2
Congenital cerebellar cortical atrophy Is a Cerebellar degeneration true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial febrile convulsions Is a False Congenital cerebellar cortical atrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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