AutoICD API

81854-2

Laboratory

CYP21A2 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

LOINC 6-Axis Classification

Component

CYP21A2 gene mutation analysis limited to known familial mutations

Property

Find

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Doc

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

CYP21A2 Fam Mut Anl Bld/T

Display Name

CYP21A2 gene familial mut analysis Molgen Doc (Bld/Tiss)

Related Names

21 Hydroxylase DeficiencyBloodCA21HCAH1Congenital adrenal hyperplasiaCPS1CYP21CYP21Bcytochrome P450, family 21, subfamily A, polypeptide 2DocumentFam Mut AnlFindingFindingsGeneticsHeredityHeritableInheritedLMTEDLTDMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMutationMutationsMutsP450c21BPCRPoint in timeRandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 81854-2?

LOINC code 81854-2 identifies "CYP21A2 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method". It measures CYP21A2 gene mutation analysis limited to known familial mutations in Bld/Tiss.

What does 81854-2 measure?

This code measures CYP21A2 gene mutation analysis limited to known familial mutations in Bld/Tiss. It belongs to the MOLPATH.MUT class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.