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63051000000105: Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Jun 2019. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module
1088791000000114 Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure) en Fully specified name Active Entire term case insensitive SNOMED CT United Kingdom clinical extension module
1088801000000113 Germline WGS (whole genome sequencing) targeting childhood onset hereditary ataxia and cerebellar anomalies panel en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure) Method Evaluation - action false Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure) Is a Germline whole genome sequencing (procedure) true Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure) Method Evaluation - action true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for childhood onset hereditary ataxia (procedure) Is a True Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure) Inferred relationship Existential restriction modifier
Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel for cerebellar anomalies (procedure) Is a True Germline whole genome sequencing targeting childhood onset hereditary ataxia and cerebellar anomalies panel (procedure) Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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