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715821000: lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type D (aandoening)


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
3303816012 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303817015 Lissencephaly with cerebellar hypoplasia type D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303818013 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
7861811000146118 lissencefalie gelijktijdig met cerebellaire hypoplasie type D nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8603131000146116 lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type D (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8603141000146112 lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type D nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3303819017 A form of lissencephaly with cerebellar hypoplasia with main features of pronounced microcephaly, intellectual disability, spastic diplegia and moderate to severe cerebellar hypoplasia involving both vermis and hemispheres. 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 D (disorder) Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) true Inferred relationship Some
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Finding site Brain structure false Inferred relationship Some 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Associated morphology Hypoplasia false Inferred relationship Some 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Occurrence Congenital false Inferred relationship Some 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Finding site Cerebellar structure false Inferred relationship Some 3
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Finding site Cerebellar structure true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Occurrence Congenital true Inferred relationship Some 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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