48732-2LOINC 2.82
NCF1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
NCF1 gene Mut Anl Bld/T
Component
- NCF1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NCF-1; NCF1A; NCF-47K; neutrophil cytosolic factor 1; Neutrophil cytosolic factor 1, (chronic granulomatous disease, autosomal 1); Nominal; NOXO2; p47phox; PCR; Point in time; Random; SH3PXD1A; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- NCF-1
- NCF-47K
- NCF1 gene targeted mutation analysis
- NCF1A
- neutrophil cytosolic factor 1
- Neutrophil cytosolic factor 1, (chronic granulomatous disease, autosomal 1)
- Nominal
- NOXO2
- p47phox
- PCR
- Point in time
- Random
- SH3PXD1A
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue