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1300188000: Congenital pontocerebellar hypoplasia type 11 (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
5298497011 Congenital pontocerebellar hypoplasia type 11 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5298498018 Pontocerebellar hypoplasia due to TBC1D23 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5298499014 PCH11 - pontocerebellar hypoplasia type 11 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5298500017 Congenital pontocerebellar hypoplasia type 11 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5298503015 A form of pontocerebellar hypoplasia characterized by microcephaly, severe global developmental delay and intellectual disability, dysmorphic facial features, cerebellar syndrome, and pontocerebellar hypoplasia on brain imaging. Behavioral abnormalities are frequently observed. Other reported manifestations include seizures, ocular anomalies, recurrent respiratory infections, and thin or absent corpus callosum, among others. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5298504014 A form of pontocerebellar hypoplasia characterised by microcephaly, severe global developmental delay and intellectual disability, dysmorphic facial features, cerebellar syndrome, and pontocerebellar hypoplasia on brain imaging. Behavioural abnormalities are frequently observed. Other reported manifestations include seizures, ocular anomalies, recurrent respiratory infections, and thin or absent corpus callosum, among others. 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 11 (disorder) Is a Intellectual disability true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Microcephaly (finding) true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Global developmental delay true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Congenital pontocerebellar hypoplasia true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital pontocerebellar hypoplasia type 11 (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 4
Congenital pontocerebellar hypoplasia type 11 (disorder) Has interpretation Impaired true Inferred relationship Some 4
Congenital pontocerebellar hypoplasia type 11 (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 5
Congenital pontocerebellar hypoplasia type 11 (disorder) Has interpretation Impaired true Inferred relationship Some 5
Congenital pontocerebellar hypoplasia type 11 (disorder) Interprets Head circumference true Inferred relationship Some 6
Congenital pontocerebellar hypoplasia type 11 (disorder) Has interpretation Below reference range true Inferred relationship Some 6
Congenital pontocerebellar hypoplasia type 11 (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 11 (disorder) Finding site Face structure true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 11 (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 11 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital pontocerebellar hypoplasia type 11 (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 11 (disorder) Finding site Cerebellar structure true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 11 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 11 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital pontocerebellar hypoplasia type 11 (disorder) Occurrence Congenital true Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 11 (disorder) Finding site Pontine structure true Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 11 (disorder) Associated morphology Hypoplasia true Inferred relationship Some 3
Congenital pontocerebellar hypoplasia type 11 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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