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1300191000: Congenital pontocerebellar hypoplasia type 13 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5298512018 Congenital pontocerebellar hypoplasia type 13 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5298513011 PCH13 - pontocerebellar hypoplasia type 13 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5298514017 Congenital pontocerebellar hypoplasia type 13 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5298515016 A form of pontocerebellar hypoplasia with characteristics of infantile onset of severe global developmental delay with absent speech, hypotonia, feeding problems, dysmorphic craniofacial features, and development of pontocerebellar hypoplasia on brain imaging later in childhood. Other structural abnormalities of the brain, which may already be apparent at an earlier stage, include small hippocampus, thin corpus callosum, periventricular white matter abnormalities, and Dandy-Walker malformation. Seizures, nystagmus, and cortical visual impairment have been reported in some cases. 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 13 Is a Global developmental delay true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 13 Is a Developmental hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 13 Is a Hereditary disorder of nervous system true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 13 Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 13 Is a Multiple system malformation syndrome true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 13 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 13 Occurrence Congenital true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 13 Finding site Cerebellar structure true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 13 Associated morphology Hypoplasia true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 13 Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 13 Occurrence Congenital true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 13 Finding site Pontine structure true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 13 Associated morphology Hypoplasia true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 13 Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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