53841-3LOINC 2.82
ATRX gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
ATRX gene Mut Anl Bld/T
Component
- ATRX gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- alpha thalassemia/mental retardation syndrome X-linked; ATP-dependent helicase ATRX; ATR2; Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; JMS; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRXHF1; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; RAD54; RAD54L; Random; SFM1; SHS; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; XH2; X-linked helicase II; X-linked nuclear protein; XNP; Zinc finger helicase; Znf-HX
Index terms
- alpha thalassemia/mental retardation syndrome X-linked
- ATP-dependent helicase ATRX
- ATR2
- ATRX gene targeted mutation analysis
- Blood
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- JMS
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MRXHF1
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- RAD54
- RAD54L
- Random
- SFM1
- SHS
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue
- X-linked helicase II
- X-linked nuclear protein
- XH2
- XNP
- Zinc finger helicase
- Znf-HX