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715463008: Congenital pontocerebellar hypoplasia type 2 (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3302712012 Congenital pontocerebellar hypoplasia type 2 en Synonym Active Case insensitive SNOMED CT core
3302713019 PCH2 - pontocerebellar hypoplasia type 2 en Synonym Active Case sensitive SNOMED CT core
3302714013 Pontocerebellar hypoplasia type 2 en Synonym Active Case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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