NIPA1 and REEP1 gene full mutation analysis in Blood or Tissue by Sequencing 81884-9
LOINC Code
LOINC code | 81884-9 | ||
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name | NIPA1 and REEP1 gene full mutation analysis in Blood or Tissue by Sequencing | ||
description | Mutation analysis of the REEP1 (SPG31) and NIPA1 genes is performed in patients with an autosomal dominant inheritance pattern of a hereditary spastic paraplegia (HSP), especially if no mutation is found in the SPAST (SPG4) or ALT1 (SPG3A) genes. The submitter's lab performs mutation analysis of exons 1-7 and flanking intronic regions of the REEP1 gene and exons 2-5 and flanking intronic regions of the NIPA1 gene by sequencing methods. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | NIPA1 gene & REEP1 gene full mutation analysis | ||
property | Find = Finding | ||
time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
system | Bld/Tiss Bld = Whole blood Tiss = Tissue, unspecified | ||
scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
method | Sequencing | ||
Additional Names | |||
short name | NIPA1+REEP1 Full Mut Anl Bld/T Seq | ||
Basic Attributes | |||
class | MOLPATH.MUT | ||
type | 1 Laboratory | ||
order vs. observation | Both | ||
Ask At Order Entry | |||
Ask at Order Entry (AOE) observations for a clinical observation or laboratory test. A LOINC term may represent a single AOE observation or a panel containing several AOE observations.
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Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
first released | |||
last updated | 2.65 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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