41116-5LOINC 2.82
ATP7A gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
ATP7A gene Mut Anl Bld/T
Component
- ATP7A gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- ATPase, Cu++ transporting, alpha polypeptide; Blood; DSMAX; Genetics; Heredity; Heritable; Identity or presence; Inherited; MC1; Menkes syndrome; MK; MNK; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; Occipital horn syndrome; OHS; PCR; Point in time; Random; SMAX3; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- ATP7A gene targeted mutation analysis
- ATPase, Cu++ transporting, alpha polypeptide
- Blood
- DSMAX
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- MC1
- Menkes syndrome
- MK
- MNK
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- Occipital horn syndrome
- OHS
- PCR
- Point in time
- Random
- SMAX3
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue