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718607001: Congenital pontocerebellar hypoplasia type 5 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3312907013 Congenital pontocerebellar hypoplasia type 5 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3312908015 Congenital pontocerebellar hypoplasia type 5 en Synonym Active Entire term case insensitive SNOMED CT core module
3312909011 PCH5 - pontocerebellar hypoplasia type 5 en Synonym Active Entire term case sensitive SNOMED CT core module
3312910018 Pontocerebellar hypoplasia type 5 en Synonym Active Entire term case insensitive SNOMED CT core module
3312911019 Fetal onset olivopontocerebellar hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module
3312912014 Foetal onset olivopontocerebellar hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pontocerebellar hypoplasia type 5 Is a Congenital pontocerebellar hypoplasia true Inferred relationship Existential restriction modifier
Congenital pontocerebellar hypoplasia type 5 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital pontocerebellar hypoplasia type 5 Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Congenital pontocerebellar hypoplasia type 5 Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 5 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 5 Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 5 Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 5 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 5 Finding site Pontine structure false Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 5 Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 5 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 5 Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 5 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 5 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 5 Finding site Pontine structure true Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 5 Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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