38537-7LOINC 2.82
ARX gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
ARX gene Mut Anl Bld/T
Component
- ARX gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- aristaless related homeobox; Aristaless-related homeobox, X-linked; Blood; CT121; EIEE1; Genetics; Heredity; Heritable; HGNC:9496; Identity or presence; Infantile spasm syndrome, X-linked; Inherited; ISSX; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRX29; MRX32; MRX33; MRX36; MRX38; MRX43; MRX54; MRX76; MRX87; MRXS1; Mut; Mut Anl; Mutations; Nominal; Partington X-linked mental retardation syndrome; PCR; Point in time; PRTS; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- aristaless related homeobox
- Aristaless-related homeobox, X-linked
- ARX gene targeted mutation analysis
- Blood
- CT121
- EIEE1
- Genetics
- Heredity
- Heritable
- HGNC:9496
- Identity or presence
- Infantile spasm syndrome, X-linked
- Inherited
- ISSX
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MRX29
- MRX32
- MRX33
- MRX36
- MRX38
- MRX43
- MRX54
- MRX76
- MRX87
- MRXS1
- Mut
- Mut Anl
- Mutations
- Nominal
- Partington X-linked mental retardation syndrome
- PCR
- Point in time
- PRTS
- Random
- Tissue
- Tissue, unspecified
- WB
2 further terms