77120-4LOINC 2.82
RPGR gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
RPGR Fam Mut Anl Bld/T
Component
- RPGR gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- Blood; COD1; CORDX1; CRD; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; orf15; PCDX; PCR; Point in time; Random; retinitis pigmentosa GTPase regulator; RP15; RP3; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; X-linked retinitis pigmentosa; XLRP3
Index terms
- Blood
- COD1
- CORDX1
- CRD
- Document
- Fam Mut Anl
- Finding
- Findings
- Genetics
- Heredity
- Heritable
- Inherited
- LMTED
- LTD
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutation
- Mutations
- Muts
- orf15
- PCDX
- PCR
- Point in time
- Random
- retinitis pigmentosa GTPase regulator
- RP15
- RP3
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue
- X-linked retinitis pigmentosa
- XLRP3