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715822007: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303822015 Lissencephaly with cerebellar hypoplasia type F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303824019 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303825018 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5401122013 A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401123015 A severe form of lissencephaly with cerebellar hypoplasia, characterised by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303822015 Lissencephaly with cerebellar hypoplasia type F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303824019 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303825018 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303823013 A severe form of lissencephaly with cerebellar hypoplasia with main features microcephaly of at least 3 standard deviations and a thick cortex associated with complete absence of the corpus callosum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401122013 A severe form of lissencephaly with cerebellar hypoplasia, characterized by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401123015 A severe form of lissencephaly with cerebellar hypoplasia, characterised by a microcephaly of at least - 3 SD and a thick cortex associated with complete absence of the corpus callosum. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3441711001000110 Lissenzephalie mit zerebellärer Hypoplasie Typ F de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366481000241117 lissencéphalie avec hypoplasie cérébelleuse congénitale de type F fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366491000241115 LCHf - lissencéphalie avec hypoplasie cérébelleuse de type F fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366481000241117 lissencéphalie avec hypoplasie cérébelleuse congénitale de type F fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6366491000241115 LCHf - lissencéphalie avec hypoplasie cérébelleuse de type F fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3441711001000110 Lissenzephalie mit zerebellärer Hypoplasie Typ F 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 F Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Lissencephaly with cerebellar hypoplasia type F Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lissencephaly with cerebellar hypoplasia type F Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Lissencephaly with cerebellar hypoplasia type F Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Lissencephaly with cerebellar hypoplasia type F Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Lissencephaly with cerebellar hypoplasia type F Finding site Cerebellar structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Lissencephaly with cerebellar hypoplasia type F Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly with cerebellar hypoplasia type F Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly with cerebellar hypoplasia type F Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Lissencephaly with cerebellar hypoplasia type F Occurrence Congenital 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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