30005-3LOINC 2.82
CYP21A2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
CYP21A2 Mut Anl Bld/T
Component
- CYP21A2 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- 21 Hydroxylase Deficiency; Blood; CA21H; CAH1; Congenital adrenal hyperplasia; CPS1; CYP21; CYP21B; cytochrome P450, family 21, subfamily A, polypeptide 2; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; P450c21B; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- 21 Hydroxylase Deficiency
- Blood
- CA21H
- CAH1
- Congenital adrenal hyperplasia
- CPS1
- CYP21
- CYP21A2 gene targeted mutation analysis
- CYP21B
- cytochrome P450, family 21, subfamily A, polypeptide 2
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- P450c21B
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue