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715820004: Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (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
5401118015 A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401119011 A severe form of lissencephaly with cerebellar hypoplasia characterised by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303812014 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303813016 Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303814010 Lissencephaly with cerebellar hypoplasia type C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6336161000241111 LCHc - lissencéphalie avec hypoplasie cérébelleuse de type C fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6336171000241115 lissencéphalie avec hypoplasie cérébelleuse congénitale de type C fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3432551001000114 Lissenzephalie mit zerebellärer Hypoplasie Typ C de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Is a Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) true Inferred relationship Some
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Associated morphology anomalie congénitale false Inferred relationship Some 2
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Finding site Brain structure false Inferred relationship Some 2
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Associated morphology Hypoplasia false Inferred relationship Some 3
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Occurrence Congenital false Inferred relationship Some 3
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Finding site Cerebellar structure false Inferred relationship Some 3
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Associated morphology Hypoplasia true Inferred relationship Some 1
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Occurrence Congenital true Inferred relationship Some 1
A severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death. Finding site Cerebellar structure 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)

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