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763821001: Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3644107013 Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3644108015 Porencephaly, cerebellar hypoplasia, internal malformations syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3644109011 Bonnemann Meinecke 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
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Is a Congenital cerebellar hypoplasia true Inferred relationship Existential restriction modifier
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Is a Congenital porencephaly true Inferred relationship Existential restriction modifier
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Is a Absence of the vermis true Inferred relationship Existential restriction modifier
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology Absence false Inferred relationship Existential restriction modifier 3
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site Cerebellar vermis structure false Inferred relationship Existential restriction modifier 3
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 3
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site Cerebellar structure true Inferred relationship Existential restriction modifier 3
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site Brain structure true Inferred relationship Existential restriction modifier 1
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology Congenital cavitation false Inferred relationship Existential restriction modifier 1
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site Cerebellar structure false Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology Absence true Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Finding site Cerebellar vermis structure true Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology Cystic dilatation true Inferred relationship Existential restriction modifier 1
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Is a Congenital absence of part of brain 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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