41117-3LOINC 2.82
AS+PWS gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
AS+PWS gene Mut Anl Bld/T
Component
- AS+PWS gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- 15q11-13; Angelman + Prader Willi syndrome; Arterial Stenosis; Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Prader Willi syndrome; Prader-Willi syndrome chromosome region; PWS; Random; SNRPN; Tissue; Tissue, unspecified; UBE3A; WB; Whole blood; Whole blood or Tissue
Index terms
- 15q11-13
- Angelman + Prader Willi syndrome
- Arterial Stenosis
- AS+PWS gene targeted mutation analysis
- Blood
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Prader Willi syndrome
- Prader-Willi syndrome chromosome region
- PWS
- Random
- SNRPN
- Tissue
- Tissue, unspecified
- UBE3A
- WB
- Whole blood
- Whole blood or Tissue