41042-3LOINC 2.82
WFS1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
WFS1 gene Mut Anl Bld/T
Component
- WFS1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; CTRCT41; DFNA14; DFNA38; DFNA6; DIDMOAD; Genetics; Heredity; Heritable; HGNC:13668; HGNC:2787; HGNC:2811; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; WFRS; WFS; WFSL; Whole blood; Whole blood or Tissue; Wolfram syndrome 1 (wolframin)
Index terms
- Blood
- CTRCT41
- DFNA14
- DFNA38
- DFNA6
- DIDMOAD
- Genetics
- Heredity
- Heritable
- HGNC:13668
- HGNC:2787
- HGNC:2811
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- WFRS
- WFS
- WFS1 gene targeted mutation analysis
- WFSL
- Whole blood
- Whole blood or Tissue
- Wolfram syndrome 1 (wolframin)