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1003444000: Type 3 lissencephaly (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4168264010 Type 3 lissencephaly en Synonym Active Entire term case insensitive SNOMED CT core module
4168265011 Type 3 lissencephaly (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
Type 3 lissencephaly Is a Lissencephaly true Inferred relationship Existential restriction modifier
Type 3 lissencephaly Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Type 3 lissencephaly Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Type 3 lissencephaly Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Type 3 lissencephaly Finding site Brain structure true Inferred relationship Existential restriction modifier 1
Type 3 lissencephaly Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Type 3 lissencephaly Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Type 3 lissencephaly 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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