38918-9LOINC 2.82
ABCC8 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
ABCC8 gene Mut Anl Bld/T
Component
- ABCC8 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- ABC36; ATP-binding cassette, sub-family C (CFTR/MRP), member 8; Blood; Genetics; Heredity; Heritable; HHF1; HI; HRINS; Hyperinsulinemia; Hyperinsulinism; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRP8; Mut; Mut Anl; Mutations; Nominal; PCR; PHHI; Point in time; Random; Sulfonylurea receptor 1; SUR; SUR1; SUR1delta2; Tissue; Tissue, unspecified; TNDM2; WB; Whole blood; Whole blood or Tissue
Index terms
- ABC36
- ABCC8 gene targeted mutation analysis
- ATP-binding cassette, sub-family C (CFTR/MRP), member 8
- Blood
- Genetics
- Heredity
- Heritable
- HHF1
- HI
- HRINS
- Hyperinsulinemia
- Hyperinsulinism
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MRP8
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- PHHI
- Point in time
- Random
- Sulfonylurea receptor 1
- SUR
- SUR1
- SUR1delta2
- Tissue
- Tissue, unspecified
- TNDM2
- WB
- Whole blood
- Whole blood or Tissue