Amelogenesis imperfecta
Clinical Genetic Test
Help
offered by
GTR Test Accession: Help GTR000593827.1
INHERITED DISEASEORALMUSCULOSKELETAL ... View more
Registered in GTR: 2021-08-23
Last annual review date for the lab: 2024-07-23 LinkOut
At a Glance
Diagnosis
Amelogenesis imperfecta
AMBN (4q13.3); AMELX (Xp22.2); CNNM4 (2q11.2); COL17A1 (10q25.1); DLX3 (17q21.33) more...
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Not provided
Not provided
Ordering Information
Offered by: Help
Test Order Code: Help
03469
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 21
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Sequence analysis has a sensitivity and specificity of 99%
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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