41750-1LOINC 2.82
COCH gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
COCH gene Mut Anl Bld/T
Component
- COCH gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Coagulation factor C homolog, cochlin (Limulus polyphemus); COCH5B2; COCH-5B2; cochlin; Cochlin precursor; Deafness, autosomal dominant 9; DFNA31; DFNA9; Genetics; Heredity; Heritable; 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; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Coagulation factor C homolog, cochlin (Limulus polyphemus)
- COCH gene targeted mutation analysis
- COCH-5B2
- COCH5B2
- cochlin
- Cochlin precursor
- Deafness, autosomal dominant 9
- DFNA31
- DFNA9
- Genetics
- Heredity
- Heritable
- 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
- Whole blood
- Whole blood or Tissue