49707-3LOINC 2.82
KCNQ2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
KCNQ2 gene Mut Anl Bld/T
Component
- KCNQ2 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- BFNC; BFNS1; Blood; EBN; EBN1; EIEE7; ENB1; Genetics; Heredity; Heritable; HNSPC; Identity or presence; Inherited; KCNA11; KV7.2; KVEBN1; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; potassium channel, voltage gated KQT-like subfamily Q, member 2; potassium voltage-gated channel, KQT-like subfamily, member 2; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- BFNC
- BFNS1
- Blood
- EBN
- EBN1
- EIEE7
- ENB1
- Genetics
- Heredity
- Heritable
- HNSPC
- Identity or presence
- Inherited
- KCNA11
- KCNQ2 gene targeted mutation analysis
- KV7.2
- KVEBN1
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- potassium channel, voltage gated KQT-like subfamily Q, member 2
- potassium voltage-gated channel, KQT-like subfamily, member 2
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue