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


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

Descriptions:

Id Description Lang Type Status Case? Module
3303808015 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3303809011 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B en Synonym Active Only initial character case insensitive SNOMED CT core module
3303810018 Lissencephaly with cerebellar hypoplasia type B en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia true Inferred relationship Existential restriction modifier
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Finding site Brain structure false Inferred relationship Existential restriction modifier 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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