48781-9LOINC 2.82
CYP21A2 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal
CYP21A2 Mut Anl Amn
Component
- CYP21A2 gene targeted mutation analysis
Specimen / system
- Amnio fld
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- 21 Hydroxylase Deficiency; AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; CA21H; CAH1; Congenital adrenal hyperplasia; CPS1; CYP21; CYP21B; cytochrome P450, family 21, subfamily A, polypeptide 2; Genetics; Gyn; Gynecology; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; OB; ObGyn; Obstetrics; P450c21B; PCR; Point in time; Random
Index terms
- 21 Hydroxylase Deficiency
- AF
- Amn
- Amn fl
- Amnio
- Amniotic flu
- Amniotic fluid
- CA21H
- CAH1
- Congenital adrenal hyperplasia
- CPS1
- CYP21
- CYP21A2 gene targeted mutation analysis
- CYP21B
- cytochrome P450, family 21, subfamily A, polypeptide 2
- Genetics
- Gyn
- Gynecology
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- OB
- ObGyn
- Obstetrics
- P450c21B
- PCR
- Point in time
- Random