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785306007: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (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
3766860019 Lissencephaly with cerebellar hypoplasia type E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766864011 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766865012 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766863017 A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of the presence of lissencephaly with an abrupt transition, near the boundary between the frontal and parietal cortex, from frontal agyria to posterior gyral simplification, associated with cerebellar hypoplasia which predominantly affects the midline vermis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3766860019 Lissencephaly with cerebellar hypoplasia type E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766864011 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766865012 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3766863017 A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of the presence of lissencephaly with an abrupt transition, near the boundary between the frontal and parietal cortex, from frontal agyria to posterior gyral simplification, associated with cerebellar hypoplasia which predominantly affects the midline vermis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3429931001000116 Lissenzephalie mit zerebellärer Hypoplasie Typ E de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6336841000241115 LCHe - lissencéphalie avec hypoplasie cérébelleuse de type E fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6336851000241117 lissencéphalie avec hypoplasie cérébelleuse congénitale de type E fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6336841000241115 LCHe - lissencéphalie avec hypoplasie cérébelleuse de type E fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6336851000241117 lissencéphalie avec hypoplasie cérébelleuse congénitale de type E fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429931001000116 Lissenzephalie mit zerebellärer Hypoplasie Typ E 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 co-occurrent with congenital cerebellar hypoplasia type E (disorder) Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) Is a Genetic disease false Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder) Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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