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11701009: Hemicephaly (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
20216019 Hemicephaly en Synonym Active Entire term case insensitive SNOMED CT core module
20217011 Hemicephalia en Synonym Active Entire term case insensitive SNOMED CT core module
20218018 Hemicephalus en Synonym Active Entire term case insensitive SNOMED CT core module
20219014 Congenital absence of cerebrum en Synonym Active Entire term case insensitive SNOMED CT core module
684545012 Hemicephaly (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemicephaly Is a Congenital absence of part of brain true Inferred relationship Existential restriction modifier
Hemicephaly Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier 1
Hemicephaly Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Hemicephaly Associated morphology Congenital partial absence false Inferred relationship Existential restriction modifier 2
Hemicephaly Occurrence Congenital false Inferred relationship Existential restriction modifier
Hemicephaly Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Hemicephaly Finding site Brain structure false Inferred relationship Existential restriction modifier 1
Hemicephaly Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier 1
Hemicephaly Finding site Brain part false Inferred relationship Existential restriction modifier 2
Hemicephaly Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier 1
Hemicephaly Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Hemicephaly Associated morphology Congenital partial absence false Inferred relationship Existential restriction modifier 2
Hemicephaly Finding site Brain part false Inferred relationship Existential restriction modifier 2
Hemicephaly Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Hemicephaly Finding site Brain part false Inferred relationship Existential restriction modifier 3
Hemicephaly Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 3
Hemicephaly Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Hemicephaly Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Hemicephaly Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Hemicephaly Associated morphology Aplasia false Inferred relationship Existential restriction modifier 2
Hemicephaly Finding site Brain structure false Inferred relationship Existential restriction modifier 2
Hemicephaly Associated morphology Absence false Inferred relationship Existential restriction modifier 2
Hemicephaly Finding site Brain part true Inferred relationship Existential restriction modifier 1
Hemicephaly Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hemicephaly Is a Congenital brain aplasia false Inferred relationship Existential restriction modifier
Hemicephaly Is a Amyelencephalus false Inferred relationship Existential restriction modifier
Hemicephaly Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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