41055-5LOINC 2.82
SLC26A4 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
SLC26A4 gene Mut Anl Bld/T
Component
- SLC26A4 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Deafness, autosomal recessive 4; DFNB4; EVA; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; NSRD4; PCR; PDS; Pendred syndrome; Pendrin (Sodium-independent chloride/iodide transporter); Point in time; Random; solute carrier family 26 (anion exchanger), member 4; Solute carrier family 26, member 4; TDH2B; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Deafness, autosomal recessive 4
- DFNB4
- EVA
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- NSRD4
- PCR
- PDS
- Pendred syndrome
- Pendrin (Sodium-independent chloride/iodide transporter)
- Point in time
- Random
- SLC26A4 gene targeted mutation analysis
- solute carrier family 26 (anion exchanger), member 4
- Solute carrier family 26, member 4
- TDH2B
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue