21733-1LOINC 2.82
RET gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
RET gene Mut Anl Bld/T
Definition
- Hirschsprung disease;medullary thyroid carcinoma
Component
- RET gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; CDHF12; CDHR16; C-RET; Genetics; Heredity; Heritable; HSCR1; Identity or presence; Inherited; MEN2A; MEN2B; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MTC1; Multiple endocrine neoplasia type IIa; Multiple endocrine neoplasia type IIb; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; PTC; Random; ret proto-oncogene; RET51; RET-ELE1; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- C-RET
- CDHF12
- CDHR16
- Genetics
- Heredity
- Heritable
- HSCR1
- Identity or presence
- Inherited
- MEN2A
- MEN2B
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MTC1
- Multiple endocrine neoplasia type IIa
- Multiple endocrine neoplasia type IIb
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- PTC
- Random
- RET gene targeted mutation analysis
- ret proto-oncogene
- RET-ELE1
- RET51
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue