OMOP Concept 21492986
Master HL7 genetic variant reporting panel
StandardMeasurementLOINC81247-9Lab Test
Maps from
0
Descendants
63
Valid from
24 Jun 2016
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Master HL7 genetic variant reporting panel across source vocabularies.
- Genetics; Genomic; Master HL7 gen var Pnl; Molecular pathology; MOLPATH; Pan; Panel.molpath; Panl; Pnl; Point in time; Random
- HL7 遗传变异报告主控组套:-:时间点:^患者:-
- Master HL7 gen var Pnl
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(7)Roll up to these when you need a wider cohort.
Narrower concepts
(63)Included automatically when you query with descendants.
- 1Complex genetic variant panel
- 1Discrete genetic variant panel
- 1Haplotype definition panel
- 1Pharmacogenomics result panel
- 1Structural variant panel
- 1Variables that apply to the overall study
- 2Allelic phase
- 2Allelic read depth
- 2Allelic state
- 2Amino acid change (pHGVS)
- 2Amino acid change [Type]
- 2Associated phenotype
- 2Basis for allelic phase [Type]
- 2CIGAR [ID]
- 2ClinVar version [ID]
- 2Complex genetic variant [ID]
- 2Complex variant HGVS name
- 2Complex variant type
- 2COSMIC version [ID]
- 2Cytogenetic (chromosome) location
- 2dbSNP [ID]
- 2dbSNP version [ID]
- 2Deletion-duplication overall interpretation
- 2Description of ranges of DNA sequences examined
- 2Discrete genetic variant
- 2Discrete variation analysis overall interpretation
- 2DNA change (c.HGVS)
- 2DNA change type
- 2Gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal
- 2Gene studied [ID]
- 2Genetic analysis report
- 2Genetic disease assessed [ID]
- 2Genetic variant assessment
- 2Genetic variation clinical significance [Imp]
- 2Genetic variation's effect on drug efficacy
- 2Genetic variation's effect on drug metabolism
- 2Genetic variation's effect on high-risk allele
- 2Genomic allele start-end
- 2Genomic alt allele [ID]
- 2Genomic DNA change (gHGVS)
- 2Genomic ref allele [ID]
- 2Genomic reference sequence [ID]
- 2Genomic source class [Type]
- 2Genomic structural variant copy number
- 2Genotype display name
- 2Haplotype name
- 2HGVS version [ID]
- 2Human reference sequence assembly version
- 2Medication assessed [ID]
- 2Medication usage implications panel
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