Concept information
Preferred term
Molecular genetic test (procedure)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- BRCA1 mutation carrier detection test (procedure)
- BRCA2 mutation carrier detection test (procedure)
- Detection of Arg3500Gln mutation in apolipoprotein B-100 gene (procedure)
- Detection of Arg506Gln mutation in gene of coagulation factor V gene and detection of G20210A mutation in gene of coagulation factor II (procedure)
- Detection of BCR-ABL t(9;22) translocation (procedure)
- Detection of G20210A mutation in gene of coagulation factor II (procedure)
- Detection of mutation in apolipoprotein B-100 gene (procedure)
- Detection of mutation in low density lipoprotein receptor gene (procedure)
- Factor VIII mutation carrier detection test (procedure)
- Familial medullary thyroid carcinoma mutation carrier detection test (procedure)
- Huntington disease gene mutation carrier detection test (procedure)
- Multiple endocrine neoplasia type 2A mutation carrier detection test (procedure)
- Multiple endocrine neoplasia type 2B mutation carrier detection test (procedure)
- Neurofibromatosis type 1 mutation carrier detection test (procedure)
- Neurofibromatosis type 2 mutation carrier detection test (procedure)
- Quantitation of BCR-ABL t(9;22) translocation (procedure)
- RET proto-oncogene mutation analysis (procedure)
- Screen for 20 common genetic mutations of cystic fibrosis using amplification refractory mutation system polymerase chain reaction assay technique (procedure)
- Screen for 29 common genetic mutations of cystic fibrosis using amplification refractory mutation system polymerase chain reaction assay technique (procedure)
- Targeted analysis for gene mutation (procedure)
- Testing for known gene mutation in family member (procedure)
- Von Hippel-Lindau disease mutation carrier detection test (procedure)
Method
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/405825005
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