77121-2LOINC 2.82
DFNB31 gene full mutation analysis in Blood or Tissue by Sequencing
DFNB31 Full Mut Anl Bld/T Seq
Component
- DFNB31 gene full mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- Autosomal recessive non-syndromic deafness; Blood; CIP98; deafness, autosomal recessive 31; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutations; Next generation sequencing; NGS; PDZD7B; Point in time; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; USH2D; Usher syndrome; WB; Whole blood; Whole blood or Tissue; WHRN; WI
Index terms
- Autosomal recessive non-syndromic deafness
- Blood
- CIP98
- deafness, autosomal recessive 31
- Document
- Finding
- Findings
- full gene sequencing
- Full Mut Anl
- Genetics
- Heredity
- Heritable
- high-throughput sequencing
- HTS
- Inherited
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutations
- Next generation sequencing
- NGS
- PDZD7B
- Point in time
- Random
- sequencing of entire coding region
- Tissue
- Tissue, unspecified
- USH2D
- Usher syndrome
- WB
- Whole blood
- Whole blood or Tissue
- WHRN
- WI