35137-9LOINC 2.82
MECP2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
MECP2 gene Mut Anl Bld/T
Component
- MECP2 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- AUTSX3; Blood; Genetics; Heredity; Heritable; Identity or presence; Inherited; MeCP-2 protein gene; methyl CpG binding protein 2; Methyl CpG binding protein 2 gene; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRX16; MRX79; MRXS13; MRXSL; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; PPMX; Random; Rett syndrome; RS; RTS; RTT; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- AUTSX3
- Blood
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- MeCP-2 protein gene
- MECP2 gene targeted mutation analysis
- methyl CpG binding protein 2
- Methyl CpG binding protein 2 gene
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MRX16
- MRX79
- MRXS13
- MRXSL
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- PPMX
- Random
- Rett syndrome
- RS
- RTS
- RTT
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue