AutoICD API

38922-1

Laboratory

PTCH gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

PTCH gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Bld/Tiss

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

PTCH gene Mut Anl Bld/T

Display Name

PTCH gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

BCNSBloodGeneticsGorlin syndromeHeredityHeritableHPE7Identity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNBCCSNevoid basal cell carcinoma syndromeNominalPatched (Drosophila) homologpatched 1PCRPoint in timePTCPTC1PTCHPTCH11RandomTissueTissue, unspecifiedWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 38922-1?

LOINC code 38922-1 identifies "PTCH gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures PTCH gene targeted mutation analysis in Bld/Tiss.

What does 38922-1 measure?

This code measures PTCH gene targeted mutation analysis 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.