FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

715819005: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (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
3303808015 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303809011 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303810018 Lissencephaly with cerebellar hypoplasia type B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 B (disorder) Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) true Inferred relationship Some
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Associated morphology anomalie congénitale false Inferred relationship Some 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Finding site Brain structure false Inferred relationship Some 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Associated morphology Hypoplasia false Inferred relationship Some 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Occurrence Congenital false Inferred relationship Some 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Finding site Cerebellar structure false Inferred relationship Some 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Occurrence Congenital true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) Finding site Cerebellar structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start