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718606005: Congenital pontocerebellar hypoplasia type 6 (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312901014 Congenital pontocerebellar hypoplasia type 6 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3312902019 Congenital pontocerebellar hypoplasia type 6 en Synonym Active Case insensitive SNOMED CT core
3312903012 Pontocerebellar hypoplasia type 6 en Synonym Active Case insensitive SNOMED CT core
3312904018 PCH6 - pontocerebellar hypoplasia type 6 en Synonym Active Case sensitive SNOMED CT core
3312905017 Fatal infantile encephalopathy with mitochondrial respiratory chain defect en Synonym Active Case insensitive SNOMED CT core
3312913016 A rare form of pontocerebellar hypoplasia with characteristics at birth of hypotonia, clonus, epilepsy, impaired swallowing and from infancy progressive microcephaly, spasticity and lactic acidosis. Reported in less than 10 cases to date. Caused by missense and splice site mutations in the mitochondrial arginyl-transfer RNA synthetase (RARS2) gene located to 6q16.1. Prognosis is poor, exact life expectancy is unknown but in most cases does not exceed infancy. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pontocerebellar hypoplasia type 6 Associated morphology Hypoplasia true Inferred relationship Some 1
Pontocerebellar hypoplasia type 6 Occurrence Congenital true Inferred relationship Some 1
Pontocerebellar hypoplasia type 6 Finding site Pontine structure true Inferred relationship Some 1
Pontocerebellar hypoplasia type 6 Pathological process Pathological developmental process true Inferred relationship Some 2
Pontocerebellar hypoplasia type 6 Pathological process Pathological developmental process true Inferred relationship Some 1
Pontocerebellar hypoplasia type 6 Is a Developmental hereditary disorder true Inferred relationship Some
Pontocerebellar hypoplasia type 6 Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Pontocerebellar hypoplasia type 6 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Pontocerebellar hypoplasia type 6 Is a Hereditary disorder of nervous system true Inferred relationship Some
Pontocerebellar hypoplasia type 6 Associated morphology Hypoplasia true Inferred relationship Some 2
Pontocerebellar hypoplasia type 6 Occurrence Congenital true Inferred relationship Some 2
Pontocerebellar hypoplasia type 6 Finding site Cerebellar structure true Inferred relationship Some 2
Pontocerebellar hypoplasia type 6 Associated morphology Hypoplasia false Inferred relationship Some 3
Pontocerebellar hypoplasia type 6 Occurrence Congenital false Inferred relationship Some 3
Pontocerebellar hypoplasia type 6 Finding site Pontine structure false Inferred relationship Some 2
Pontocerebellar hypoplasia type 6 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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