FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

715821000: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (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
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
5401120017 A rare form of lissencephaly with cerebellar hypoplasia characterized by pronounced microcephaly (<= -3 SD), 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
5401121018 A rare form of lissencephaly with cerebellar hypoplasia characterised by pronounced microcephaly (<= -3 SD), 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 Congenital anomaly 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

Component annotation with string value reference set (foundation metadata concept)

Back to Start