FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

1177169004: Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4643807011 Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4643808018 Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4643809014 Congenital cerebellar ataxia due to RNU12 mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4643810016 A rare hereditary ataxia with characteristics of delayed motor milestones in early infancy, hypotonia, ataxic gait, intention tremor, nystagmus, dysarthric speech and variable learning difficulties. Neuroimaging shows a mixed picture of cerebellar hypoplasia and degeneration, with an almost absent inferior lobule and thinning of the folia of the vermis. In addition, cisterna magna and fourth ventricle are enlarged with relative sparing of the brain stem volume. 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 cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Is a Intellectual disability true Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Is a Hereditary ataxia (disorder) true Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Is a Cerebellar ataxia true Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Finding site Cerebellar structure true Inferred relationship Some 1
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Is a Congenital cerebellar hypoplasia true Inferred relationship Some
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 2
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Has interpretation Impaired true Inferred relationship Some 2
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 3
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Has interpretation Impaired true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start