41073-8LOINC 2.82
NR0B1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
NR0B1 gene Mut Anl Bld/T
Component
- NR0B1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Adrenal hypoplasia congenita; AHC; AHCH; AHCX; AHX; Blood; DAX1; DAX-1; DSS; Genetics; GTD; Heredity; Heritable; HHG; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; NROB1; nuclear receptor subfamily 0, group B, member 1; PCR; Point in time; Random; SRXY2; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Adrenal hypoplasia congenita
- AHC
- AHCH
- AHCX
- AHX
- Blood
- DAX-1
- DAX1
- DSS
- Genetics
- GTD
- Heredity
- Heritable
- HHG
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- NR0B1 gene targeted mutation analysis
- NROB1
- nuclear receptor subfamily 0, group B, member 1
- PCR
- Point in time
- Random
- SRXY2
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue