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718607001: Congenital pontocerebellar hypoplasia type 5 (disorder)


Status: current, Not 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
3312907013 Congenital pontocerebellar hypoplasia type 5 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312908015 Congenital pontocerebellar hypoplasia type 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312909011 PCH5 - pontocerebellar hypoplasia type 5 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312910018 Pontocerebellar hypoplasia type 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312911019 Fetal onset olivopontocerebellar hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312912014 Foetal onset olivopontocerebellar hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital pontocerebellar hypoplasia type 5 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 5 (disorder) morphologie associée (attribut) Hypoplasia (morphologic abnormality) true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 5 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 5 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 5 (disorder) localisation d'une constatation (attribut) Pontine structure true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 5 (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 5 (disorder) est un(e) (attribut) Congenital pontocerebellar hypoplasia true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 5 (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 5 (disorder) est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 5 (disorder) morphologie associée (attribut) Hypoplasia (morphologic abnormality) true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 5 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 5 (disorder) localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 5 (disorder) morphologie associée (attribut) Hypoplasia (morphologic abnormality) false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 5 (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 5 (disorder) localisation d'une constatation (attribut) Pontine structure false Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 5 (disorder) localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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