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1162839003: XK aprosencephaly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4591719016 XK aprosencephaly syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4591720010 XK aprosencephaly syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4591721014 XK syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
4591722019 Garcia Lurie 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
XK aprosencephaly syndrome Is a Aprosencephaly true Inferred relationship Existential restriction modifier
XK aprosencephaly syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
XK aprosencephaly syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
XK aprosencephaly syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
XK aprosencephaly syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
XK aprosencephaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
XK aprosencephaly syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 1
XK aprosencephaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
XK aprosencephaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
XK aprosencephaly syndrome Finding site Structure of diencephalon true Inferred relationship Existential restriction modifier 1
XK aprosencephaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
XK aprosencephaly syndrome Finding site Structure of telencephalon true Inferred relationship Existential restriction modifier 2
XK aprosencephaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
XK aprosencephaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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