36912-4LOINC 2.82
CATCH22 syndrome gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal
CATCH22 gene Mut Tested Bld/T
Component
- CATCH22 syndrome gene mutations tested for
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; CATCH22 gene; DGS; DiGeorge Syndrome; Gene mut tested; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Tested; Mutation; Muts; Nominal; PCR; Point in time; Random; Shprintzen syndrome; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- CATCH22 gene
- DGS
- DiGeorge Syndrome
- Gene mut tested
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Tested
- Mutation
- Muts
- Nominal
- PCR
- Point in time
- Random
- Shprintzen syndrome
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue