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715463008: Congenital pontocerebellar hypoplasia type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302711017 Congenital pontocerebellar hypoplasia type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302712012 Congenital pontocerebellar hypoplasia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302713019 PCH2 - pontocerebellar hypoplasia type 2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3302714013 Pontocerebellar hypoplasia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302715014 The most common subtype of pontocerebellar hypoplasia with features of neonatal onset, lack of voluntary motor development and later progressive microencephaly, general clonus, development of chorea and spasticity.The majority of patients will not reach puberty. Inherited in an autosomal recessive manner. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


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