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715819005: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303808015 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3303809011 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B en Synonym Active Initial character case insensitive SNOMED CT core
3303810018 Lissencephaly with cerebellar hypoplasia type B en Synonym Active Initial character case insensitive SNOMED CT core
3303811019 A form of lissencephaly with cerebellar hypoplasia with main features of subtle microcephaly, hypotonia and neurological and cognitive development delay. Hippocampal malformation is a characteristic feature on imaging. 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 B Occurrence Congenital true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type B Pathological process Pathological developmental process true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type B Associated morphology Hypoplasia true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type B Finding site Cerebellar structure true Inferred relationship Some 1
Lissencephaly with cerebellar hypoplasia type B Is a Lissencephaly with cerebellar hypoplasia true Inferred relationship Some
Lissencephaly with cerebellar hypoplasia type B Associated morphology Congenital anomaly false Inferred relationship Some 2
Lissencephaly with cerebellar hypoplasia type B Finding site Brain structure false Inferred relationship Some 2
Lissencephaly with cerebellar hypoplasia type B Associated morphology Hypoplasia false Inferred relationship Some 3
Lissencephaly with cerebellar hypoplasia type B Occurrence Congenital false Inferred relationship Some 3
Lissencephaly with cerebellar hypoplasia type B 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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