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


Status: current, Primitive. 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 Active Initial character case insensitive SNOMED CT core
3766867016 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3766868014 Lissencephaly with cerebellar hypoplasia type A en Synonym Active Initial character case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Finding site Cerebellar structure true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Associated morphology Hypoplasia true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Is a Lissencephaly with cerebellar hypoplasia true Inferred relationship Some
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Is a Genetic disease false Inferred relationship Some
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Occurrence Congenital true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Pathological process Pathological developmental process true Inferred relationship Some 1

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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