• Magnesium/Creatinine Ratio, Random, Urine
  • Helicobacter pylori Culture with Antimicrobial Susceptibilities
  • Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
  • Growth Hormone Binding Protein (GHBP)
  • PDGFRB/TEL Translocation (5;12) for Chronic Myelomonocytic Leukemia, FISH, Blood
  • Anaplastic Lymphoma Kinase (ALK) Gene Rearrangements, FISH, Tissue
  • Smith (ENA) Antibody, IgG
  • Acetylcholine Receptor (AChR) Antibody
  • RFC1 (replication factor C subunit 1) Gene Mutation Analysis
  • Herpesvirus 6 (HHV-6) Antibody, IgM
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Medical Test

CPT
Access to Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants is restricted.
Loading...