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785307003: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder)


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
3766866013 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766867016 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766868014 Lissencephaly with cerebellar hypoplasia type A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766869018 A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3777424013 A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical grey matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3766866013 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766867016 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766868014 Lissencephaly with cerebellar hypoplasia type A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766869018 A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3777424013 A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical grey matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable predominantly midline cerebellar hypoplasia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3416421001000112 Lissenzephalie mit zerebellärer Hypoplasie Typ A de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6387481000241117 LCHa - lissencéphalie avec hypoplasie cérébelleuse de type A fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6387491000241115 lissencéphalie avec hypoplasie cérébelleuse congénitale de type A fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6387481000241117 LCHa - lissencéphalie avec hypoplasie cérébelleuse de type A fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6387491000241115 lissencéphalie avec hypoplasie cérébelleuse congénitale de type A fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3416421001000112 Lissenzephalie mit zerebellärer Hypoplasie Typ A 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 with cerebellar hypoplasia type A Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly with cerebellar hypoplasia type A Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly with cerebellar hypoplasia type A Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly with cerebellar hypoplasia type A Is a Genetic disease false Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly with cerebellar hypoplasia type A Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly with cerebellar hypoplasia type A Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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