AutoICD API

35744-2

Laboratory

TP73L gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

TP73L 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

TP73L gene Mut Anl Bld/T

Display Name

TP73L gene targeted mutation analysis Molgen Nom (Bld/Tiss)

Related Names

AISB(p51A)B(p51B)BloodEctrodactyly, ectodermal dysplasia, and cleft lip/palate syndromeEEC dysplasiaEEC3GeneticsHeredityHeritableHGNC:15979Identity or presenceInheritedKETLMSMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNBPNominalOFC8p40p51p53CPp63p73Hp73LPCRPoint in timeRandomRHSSHFM4TissueTissue, unspecifiedTP53CPTP53LTP63TP73LTumor protein 63 kDa with strong homology to p53 genetumor protein p63Tumor protein p73-like geneWBWhole bloodWhole blood or Tissue

Frequently Asked Questions

What is LOINC code 35744-2?

LOINC code 35744-2 identifies "TP73L gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal". It measures TP73L gene targeted mutation analysis in Bld/Tiss.

What does 35744-2 measure?

This code measures TP73L 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.