OMOP Concept 36032346
ATP7B gene full mutation analysis in Blood or Tissue by Sequencing
StandardMeasurementLOINC95781-1Lab Test
Maps from
0
Descendants
0
Valid from
15 Dec 2020
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Synonyms
Alternative names recorded for ATP7B gene full mutation analysis in Blood or Tissue by Sequencing across source vocabularies.
- ATP7B gene Full Mut Anl Bld/T Seq
- ATP7B gene variant analysis, Blood or tissue specimen
- ATP7B 基因 全面突变分析:发现:时间点:全血/组织:文档型:序列测定
- ATPase gene; ATPase, Cu++ transporting, beta polypeptide; Blood; CU(2+)- transporting beta polypeptide; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; Point in time; PWD; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; WB; WC1; WD; Whole blood; Whole blood or Tissue; Wilson disease; WND
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Get this concept via the API
Resolve ATP7B gene full mutation analysis in Blood or Tissue by Sequencing - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/36032346?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card