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718611007: Congenital pontocerebellar hypoplasia type 8 (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
3312932010 Congenital pontocerebellar hypoplasia type 8 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312933017 Congenital pontocerebellar hypoplasia type 8 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312934011 PCH8 - pontocerebellar hypoplasia type 8 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312935012 Pontocerebellar hypoplasia type 8 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312936013 Pontocerebellar hypoplasia due to CHMP1A (charged multivesicular body protein 1A) mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5401794013 Pontocerebellar hypoplasia type 8 (PCH8) is a novel very rare form of pontocerebellar hypoplasia characterized clinically by progressive microencephaly, feeding difficulties, severe developmental delay, although walking may be achieved, hypotonia often associated with increased muscle tone of lower extremities and deep tendon reflexes, joint deformities in the lower extremities, and occasionally complex seizures. PCH8 is caused by a loss-of-function mutation in the CHMP1A gene. MRI demonstrates a pontocerebellar hypoplasia with vermis and hemispheres equally affected and mild to severely reduced cerebral white matter volume with a fully formed very thin corpus callosum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401795014 Pontocerebellar hypoplasia type 8 (PCH8) is a novel very rare form of pontocerebellar hypoplasia characterised clinically by progressive microencephaly, feeding difficulties, severe developmental delay, although walking may be achieved, hypotonia often associated with increased muscle tone of lower extremities and deep tendon reflexes, joint deformities in the lower extremities, and occasionally complex seizures. PCH8 is caused by a loss-of-function mutation in the CHMP1A gene. MRI demonstrates a pontocerebellar hypoplasia with vermis and hemispheres equally affected and mild to severely reduced cerebral white matter volume with a fully formed very thin corpus callosum. 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 8 (disorder) Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 8 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 8 (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 8 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 8 (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 8 (disorder) Finding site Cerebellar structure true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 8 (disorder) Associated morphology Hypoplasia false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 8 (disorder) Occurrence Congenital false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 8 (disorder) Finding site Pontine structure false Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 8 (disorder) Finding site Cerebellar structure false Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 8 (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 8 (disorder) Finding site Pontine structure true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 8 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 8 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 8 (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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