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718719001: Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3313323010 Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313324016 Lissencephaly type 3 familial fetal akinesia sequence syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313329014 Lissencephaly type 3 familial foetal akinesia sequence syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401835019 Lissencephaly type 3-familial fetal akinesia sequence syndrome is characterized by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. Less than 10 cases have been described so far. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and lissencephaly type III with metacarpal bone dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401836018 Lissencephaly type 3-familial fetal akinesia sequence syndrome is characterised by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. Less than 10 cases have been described so far. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and lissencephaly type III with metacarpal bone dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3313323010 Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313323010 Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313324016 Lissencephaly type 3 familial fetal akinesia sequence syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313324016 Lissencephaly type 3 familial fetal akinesia sequence syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313329014 Lissencephaly type 3 familial foetal akinesia sequence syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3313329014 Lissencephaly type 3 familial foetal akinesia sequence syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3313330016 This syndrome has characteristics of the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. Less than 10 cases have been described so far. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and lissencephaly type III with metacarpal bone dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401835019 Lissencephaly type 3-familial fetal akinesia sequence syndrome is characterized by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. Less than 10 cases have been described so far. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and lissencephaly type III with metacarpal bone dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401836018 Lissencephaly type 3-familial fetal akinesia sequence syndrome is characterised by the association of microencephaly, agenesis of the corpus callosum, brainstem hypoplasia, cystic cerebellum and fetal akinesia sequence. Less than 10 cases have been described so far. The syndrome is transmitted as an autosomal recessive trait and may be an allelic variant of Neu-Laxova syndrome and lissencephaly type III with metacarpal bone dysplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3451601001000117 Lissenzephalie Typ III - familiäre fetale Akinesie/Hypokinesie-Sequenz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887031000172116 syndrome de lissencéphalie type 3-séquence d'akinésie foetale familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
887031000172116 syndrome de lissencéphalie type 3-séquence d'akinésie foetale familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451601001000117 Lissenzephalie Typ III - familiäre fetale Akinesie/Hypokinesie-Sequenz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Is a Lissencephaly false Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 3
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Is a Microlissencephaly true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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