41115-7LOINC 2.82
NOD2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
NOD2 gene Mut Anl Bld/T
Component
- NOD2 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- ACUG; Arthrocutaneouveal granulomatosis (Blau syndrome); BLAU; Blau syndrome, granulomatous synovitis with uveitis and cranial neuropathies; Blood; CARD15; Caspase recruitment domain family, member 15; CD; CLR16.3; Crohn disease; Genetics; Heredity; Heritable; IBD1; Identity or presence; Inflammatory bowel disease 1; Inherited; LRR-containing protein gene; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NLRC2; NOD2; NOD2B; Nominal; nucleotide-binding oligomerization domain containing 2; Nucleotide-binding oligomerization domain protein 2 gene; PCR; Point in time; PSORAS1; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- ACUG
- Arthrocutaneouveal granulomatosis (Blau syndrome)
- BLAU
- Blau syndrome, granulomatous synovitis with uveitis and cranial neuropathies
- Blood
- CARD15
- Caspase recruitment domain family, member 15
- CD
- CLR16.3
- Crohn disease
- Genetics
- Heredity
- Heritable
- IBD1
- Identity or presence
- Inflammatory bowel disease 1
- Inherited
- LRR-containing protein gene
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- NLRC2
- NOD2
- NOD2 gene targeted mutation analysis
- NOD2B
- Nominal
- nucleotide-binding oligomerization domain containing 2
- Nucleotide-binding oligomerization domain protein 2 gene
- PCR
- Point in time
- PSORAS1
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
1 further terms