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718606005: pontocerebellaire hypoplasie type 6 (aandoening)


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
3312901014 Congenital pontocerebellar hypoplasia type 6 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312902019 Congenital pontocerebellar hypoplasia type 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312903012 Pontocerebellar hypoplasia type 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312904018 PCH6 - pontocerebellar hypoplasia type 6 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312905017 Fatal infantile encephalopathy with mitochondrial respiratory chain defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6430641000146112 pontocerebellaire hypoplasie type 6 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6430651000146110 pontocerebellaire hypoplasie type 6 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6430661000146113 PCH6 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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 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 6 (disorder) Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 6 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 6 (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 6 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 6 (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 6 (disorder) Finding site Cerebellar structure true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 6 (disorder) Associated morphology Hypoplasia false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 6 (disorder) Occurrence Congenital false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 6 (disorder) Finding site Pontine structure false Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 6 (disorder) Finding site Cerebellar structure false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 6 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 6 (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 6 (disorder) Finding site Pontine structure true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 6 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 6 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 6 (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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