77128-7LOINC 2.82
USH1C gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
USH1C Fam Mut Anl Bld/T
Component
- USH1C gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- AIE-75; Blood; DFNB18; DFNB18A; Document; Fam Mut Anl; Finding; Findings; Genetics; harmonin; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; Non-syndromic sensorineural deafness autosomal recessive type 18; NY-CO-37; NY-CO-38; PCR; PDZ-45; PDZ73; PDZ-73; PDZ-73/NY-CO-38; PDZD7C; Point in time; Random; Tissue; Tissue, unspecified; ush1cpst; Usher syndrome 1C (autosomal recessive, severe); Usher syndrome type 1C; WB; Whole blood; Whole blood or Tissue
Index terms
- AIE-75
- Blood
- DFNB18
- DFNB18A
- Document
- Fam Mut Anl
- Finding
- Findings
- Genetics
- harmonin
- Heredity
- Heritable
- Inherited
- LMTED
- LTD
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutation
- Mutations
- Muts
- Non-syndromic sensorineural deafness autosomal recessive type 18
- NY-CO-37
- NY-CO-38
- PCR
- PDZ-45
- PDZ-73
- PDZ-73/NY-CO-38
- PDZ73
- PDZD7C
- Point in time
- Random
- Tissue
- Tissue, unspecified
- ush1cpst
- Usher syndrome 1C (autosomal recessive, severe)
- Usher syndrome type 1C
- WB
2 further terms