AutoICD API

48781-9

Laboratory

CYP21A2 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal

LOINC 6-Axis Classification

Component

CYP21A2 gene targeted mutation analysis

Property

Prid

Time Aspect

Pt

System

Amnio fld

Scale Type

Nom

Method Type

Molgen

Details

Class

MOLPATH.MUT

Order/Observation

Both

Short Name

CYP21A2 Mut Anl Amn

Display Name

CYP21A2 gene targeted mutation analysis Molgen Nom (Amn fld)

Related Names

21 Hydroxylase DeficiencyAFAmnAmn flAmnioAmniotic fluAmniotic fluidCA21HCAH1Congenital adrenal hyperplasiaCPS1CYP21CYP21Bcytochrome P450, family 21, subfamily A, polypeptide 2GeneticsGynGynecologyHeredityHeritableIdentity or presenceInheritedMolecular geneticsMolecular pathologyMOLPATHMOLPATH.MUTATIONSMutMut AnlMutationsNominalOBObGynObstetricsP450c21BPCRPoint in timeRandom

Frequently Asked Questions

What is LOINC code 48781-9?

LOINC code 48781-9 identifies "CYP21A2 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal". It measures CYP21A2 gene targeted mutation analysis in Amnio fld.

What does 48781-9 measure?

This code measures CYP21A2 gene targeted mutation analysis in Amnio fld. 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.