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


Status: current, Primitive. 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 Active Initial character case insensitive SNOMED CT core
3303824019 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3303825018 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F en Synonym Active Initial character case insensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lissencephaly with cerebellar hypoplasia type F Associated morphology Hypoplasia true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type F Pathological process Pathological developmental process true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type F Finding site Cerebellar structure true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type F Occurrence Congenital true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type F Is a Lissencephaly with cerebellar hypoplasia true Inferred relationship Some
Lissencephaly with cerebellar hypoplasia type F Associated morphology Congenital anomaly false Inferred relationship Some 2
Lissencephaly with cerebellar hypoplasia type F Finding site Brain structure false Inferred relationship Some 2
Lissencephaly with cerebellar hypoplasia type F Associated morphology Hypoplasia false Inferred relationship Some 3
Lissencephaly with cerebellar hypoplasia type F Occurrence Congenital false Inferred relationship Some 3
Lissencephaly with cerebellar hypoplasia type F Finding site Cerebellar structure false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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