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770560008: Lissencephaly due to LIS1 mutation (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
3701271018 PAFAH1B1-related lissencephaly en Synonym Active Entire term case sensitive SNOMED CT core module
3701273015 PAFAH1B1 (platelet activating factor acetylhydrolase 1b regulatory subunit 1) related lissencephaly en Synonym Active Entire term case sensitive SNOMED CT core module
3701275010 Lissencephaly due to LIS1 mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
3701279016 Lissencephaly due to LIS1 mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lissencephaly due to LIS1 mutation Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Lissencephaly due to LIS1 mutation Is a Anomalies of cerebrum false Inferred relationship Existential restriction modifier
Lissencephaly due to LIS1 mutation Is a Type 1 lissencephaly true Inferred relationship Existential restriction modifier
Lissencephaly due to LIS1 mutation Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Lissencephaly due to LIS1 mutation Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Lissencephaly due to LIS1 mutation Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Lissencephaly due to LIS1 mutation Is a Congenital anomaly of cerebrum 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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