77126-1LOINC 2.82
PCDH15 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
PCDH15 Fam Mut Anl Bld/T
Component
- PCDH15 gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- Blood; CDHR15; DFNB23; Document; Fam Mut Anl; Finding; Findings; Genetics; hearing loss; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; PCR; Point in time; protocadherin-related 15; Random; Tissue; Tissue, unspecified; USH1F; Usher syndrome type 1F; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- CDHR15
- DFNB23
- Document
- Fam Mut Anl
- Finding
- Findings
- Genetics
- hearing loss
- Heredity
- Heritable
- Inherited
- LMTED
- LTD
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutation
- Mutations
- Muts
- PCR
- Point in time
- protocadherin-related 15
- Random
- Tissue
- Tissue, unspecified
- USH1F
- Usher syndrome type 1F
- WB
- Whole blood
- Whole blood or Tissue