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782753000: syndroom van verstandelijke beperking, grof aangezicht, macrocefalie en cerebellaire hypotrofie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3755618014 Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755619018 SCAR20 - autosomal recessive spinocerebellar ataxia type 20 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755620012 Autosomal recessive spinocerebellar ataxia type 20 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755621011 Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
8502751000146113 syndroom van verstandelijke beperking, grof aangezicht, macrocefalie en cerebellaire hypotrofie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8502761000146111 syndroom van mentale retardatie, grof aangezicht, macrocefalie en cerebellaire hypotrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8502771000146117 syndroom van verstandelijke beperking, grof aangezicht, macrocefalie en cerebellaire hypotrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8502781000146115 syndroom van verstandelijke handicap, grof aangezicht, macrocefalie en cerebellaire hypotrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8603021000146117 autosomaal recessieve spinocerebellaire ataxie type 20 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3755622016 A rare genetic central nervous system malformation syndrome with characteristics of early-onset progressive severe cerebellar ataxia associated with progressive moderate to severe intellectual disability, global developmental delay, progressively coarsening facial features, relative macrocephaly and absence of seizures. Sensorineural hearing loss may be associated. Neuroimaging reveals cerebellar atrophy/hypoplasia. There is evidence the disease is caused by homozygous mutation in the SNX14 gene on chromosome 6q14. 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
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Occurrence Congenital true Inferred relationship Some 1
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Congenital cerebellar hypoplasia true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Hereditary disorder of nervous system false Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Hereditary ataxia (disorder) true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Intellectual disability true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Occurrence Congenital true Inferred relationship Some 2
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Global developmental delay true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Early onset cerebellar ataxia true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Finding site Face structure true Inferred relationship Some 1
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Finding site Cerebellar structure true Inferred relationship Some 2
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Associated morphology Hypoplasia true Inferred relationship Some 2
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 3
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Has interpretation Impaired true Inferred relationship Some 3
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 4
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Has interpretation Impaired true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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US English

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