GTR Home > Tests > Search results - C0852654[DISCUI]

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GTR test search results for C0852654[DISCUI]

C Clinical test, R Research test

Showing 1 to 20 of 56 tests for 602 conditions in 46 labs

CAdrenal hyperplasia, congenital, due to 21-hydroxylase deficiency

Lab: Centogene AG - the Rare Disease Company Rostock, Mecklenburg-Vorpommern, Germany
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CCYP21A2 target mutation analysis

Test targets
Methods
  • X Mutation scanning of select exons
  • E Sequence analysis of select exons

CCYP21A2 gene Sequencing

Test targets
Methods
  • C Sequence analysis of the entire coding region

CCongenital Adrenal Hyperplasia due to 21-Hydroxylase deficiency

Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CCongenital Adrenal Hyperplasia (CAH)

Test targets
Methods
  • C Sequence analysis of the entire coding region

CCongenital Adrenal Hyperplasia due to 21-hydroxylase deficiency via the CYP21A2 Gene

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CCongenital Adrenal Hyperplasia Test

Lab: Asper Biotech Asper Biotech Ltd. Tartu, Tartumaa, Estonia
Test targets
Methods
  • D Deletion/duplication analysis
  • T Targeted variant analysis

CCongenital Adrenal Hyperplasia (CAH) Evaluation

Lab: Athena Diagnostics Inc Marlborough, Massachusetts, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region

CCYP21A2 (CAH) Evaluation

Lab: Athena Diagnostics Inc Marlborough, Massachusetts, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region

CCYP21A2. Complete sequencing

Lab: Instituto de Medicina Genomica Paterna, Comunidad Valenciana, Spain
Test targets
Methods
  • C Sequence analysis of the entire coding region

CCYP21A2. MLPA testing

Lab: Instituto de Medicina Genomica Paterna, Comunidad Valenciana, Spain
Test targets
Methods
  • D Deletion/duplication analysis

CCYP21A2 Sequencing

Test targets
Methods
  • C Sequence analysis of the entire coding region

CNuclear-Mito 500 NGS Panel

Lab: Fulgent Clinical Diagnostics Lab Fulgent Diagnostics Temple City, California, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (600)
Total targets (500)

CCongenital Adrenal Hyperplasia

Lab: GeneTech ATS GeneTech Private Limited Hyderabad, Andhra Pradesh, India
Test targets
Methods
  • C Sequence analysis of the entire coding region

CCongenital Adrenal Hyperplasia

Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CCYP21A2

Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CCAH (21-Hydroxylase Deficiency) Rare Mutations (NY)

Lab: Quest Diagnostics Nichols Institute San Juan Capistrano San Juan Capistrano, California, United States
Test targets
Methods
  • T Targeted variant analysis

CCAH (21-Hydroxylase Deficiency) Rare Mutations

Lab: Quest Diagnostics Nichols Institute San Juan Capistrano San Juan Capistrano, California, United States
Test targets
Methods
  • T Targeted variant analysis

CCAH (21-Hydroxylase Deficiency) Common Mutations (NY)

Lab: Quest Diagnostics Nichols Institute San Juan Capistrano San Juan Capistrano, California, United States
Test targets
Methods
  • T Targeted variant analysis

Showing 1 to 20 of 56 tests for 602 conditions in 46 labs

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