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1003374009: Microlissencephaly (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168105019 Microlissencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168106018 Microlissencephaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168105019 Microlissencephaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4168106018 Microlissencephaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3437921001000113 Mikrolissenzephalie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437921001000113 Mikrolissenzephalie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microlissencephaly Is a microcéphalie false Inferred relationship Existential restriction modifier (core metadata concept)
Microlissencephaly Is a Lissencephaly true Inferred relationship Existential restriction modifier (core metadata concept)
Microlissencephaly Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microlissencephaly Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microlissencephaly Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Microlissencephaly Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microlissencephaly Is a Congenital microencephaly true Inferred relationship Existential restriction modifier (core metadata concept)
Microlissencephaly Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Is a True Microlissencephaly Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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