41058-9LOINC 2.82
SH2D1A gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
SH2D1A gene Mut Anl Bld/T
Component
- SH2D1A gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; DSHP; Duncan disease; EBVS; Genetics; Heredity; Heritable; Identity or presence; IMD5; Inherited; Lymphoproliferative syndrome; LYP; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MTCP1; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; SAP; SAP/SH2D1A; SH2 domain containing 1A; SH2 domain protein 1A gene; Signaling lymphocyte activation molecule; SLAM; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; XLP; XLPD; XLPD1
Index terms
- Blood
- DSHP
- Duncan disease
- EBVS
- Genetics
- Heredity
- Heritable
- Identity or presence
- IMD5
- Inherited
- Lymphoproliferative syndrome
- LYP
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MTCP1
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Random
- SAP
- SAP/SH2D1A
- SH2 domain containing 1A
- SH2 domain protein 1A gene
- SH2D1A gene targeted mutation analysis
- Signaling lymphocyte activation molecule
- SLAM
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue
- XLP
- XLPD
- XLPD1