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771178004: Edinburgh malformation syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3704759012 Typus Edinburgensis en Synonym Active Only initial character case insensitive SNOMED CT core module
3704760019 Edinburgh malformation syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3704761015 Edinburgh malformation syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Edinburgh malformation syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Edinburgh malformation syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Edinburgh malformation syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Edinburgh malformation syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Edinburgh malformation syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Edinburgh malformation syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Edinburgh malformation syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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