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718611007: Congenital pontocerebellar hypoplasia type 8 (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3312933017 Congenital pontocerebellar hypoplasia type 8 en Synonym Active Case insensitive SNOMED CT core
3312934011 PCH8 - pontocerebellar hypoplasia type 8 en Synonym Active Case sensitive SNOMED CT core
3312935012 Pontocerebellar hypoplasia type 8 en Synonym Active Case insensitive SNOMED CT core
3312936013 Pontocerebellar hypoplasia due to CHMP1A (charged multivesicular body protein 1A) mutation en Synonym Active Initial character case insensitive SNOMED CT core
3312906016 A novel very rare form of PCH with clinical manifestations of progressive microcephaly, feeding difficulties and 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 are demonstrated. PCH8 is caused by a loss-of-function mutation in the CHMP1A gene. 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 8 Occurrence Congenital true Inferred relationship Some 1
Pontocerebellar hypoplasia type 8 Finding site Pontine structure true Inferred relationship Some 1
Pontocerebellar hypoplasia type 8 Associated morphology Hypoplasia true Inferred relationship Some 1
Pontocerebellar hypoplasia type 8 Pathological process Pathological developmental process true Inferred relationship Some 1
Pontocerebellar hypoplasia type 8 Pathological process Pathological developmental process true Inferred relationship Some 2
Pontocerebellar hypoplasia type 8 Is a Developmental hereditary disorder true Inferred relationship Some
Pontocerebellar hypoplasia type 8 Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Pontocerebellar hypoplasia type 8 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Pontocerebellar hypoplasia type 8 Is a Hereditary disorder of nervous system true Inferred relationship Some
Pontocerebellar hypoplasia type 8 Associated morphology Hypoplasia true Inferred relationship Some 2
Pontocerebellar hypoplasia type 8 Occurrence Congenital true Inferred relationship Some 2
Pontocerebellar hypoplasia type 8 Finding site Cerebellar structure true Inferred relationship Some 2
Pontocerebellar hypoplasia type 8 Associated morphology Hypoplasia false Inferred relationship Some 3
Pontocerebellar hypoplasia type 8 Occurrence Congenital false Inferred relationship Some 3
Pontocerebellar hypoplasia type 8 Finding site Pontine structure false Inferred relationship Some 2
Pontocerebellar hypoplasia type 8 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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