32632-2LOINC 2.82
HEXA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
HEXA gene Mut Anl Bld/T
Component
- HEXA gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- beta-N-acetylhexosaminidase gene; Blood; Genetics; GM2-gangliosidosis; Heredity; Heritable; hexosaminidase A (alpha polypeptide); hexosaminidase A (alpha polypeptide) gene; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; N-acetyl-beta-glucosaminidase gene; Nominal; PCR; Point in time; Random; Tay-Sachs disease; Tissue; Tissue, unspecified; TSD; UniversalLabOrders; WB; Whole blood; Whole blood or Tissue
Index terms
- beta-N-acetylhexosaminidase gene
- Blood
- Genetics
- GM2-gangliosidosis
- Heredity
- Heritable
- HEXA gene targeted mutation analysis
- hexosaminidase A (alpha polypeptide)
- hexosaminidase A (alpha polypeptide) gene
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- N-acetyl-beta-glucosaminidase gene
- Nominal
- PCR
- Point in time
- Random
- Tay-Sachs disease
- Tissue
- Tissue, unspecified
- TSD
- UniversalLabOrders
- WB
- Whole blood
- Whole blood or Tissue