77118-8LOINC 2.82
RPGRIP1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
RPGRIP1 Fam Mut Anl Bld/T
Component
- RPGRIP1 gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- Blood; Congenital blindness; CORD13; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LCA6; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; PCR; Point in time; Random; Retinitis pigmentosa; retinitis pigmentosa GTPase regulator interacting protein 1; RGI1; RGRIP; RPGRIP; RPGRIP1d; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Congenital blindness
- CORD13
- Document
- Fam Mut Anl
- Finding
- Findings
- Genetics
- Heredity
- Heritable
- Inherited
- LCA6
- LMTED
- LTD
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutation
- Mutations
- Muts
- PCR
- Point in time
- Random
- Retinitis pigmentosa
- retinitis pigmentosa GTPase regulator interacting protein 1
- RGI1
- RGRIP
- RPGRIP
- RPGRIP1d
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue