NGCDA - Overview: Congenital Dyserythropoietic Anemia Sequencing, Varies

Test Catalog

Test Name

Test ID: NGCDA    
Congenital Dyserythropoietic Anemia Sequencing, Varies

Useful For Suggests clinical disorders or settings where the test may be helpful

Confirmation of the diagnosis or carrier mutation status of genes associated with congenital dyserythropoietic anemia

 

Identifying mutations within genes associated with phenotypic severity, allowing for predictive testing and further genetic counseling

Genetics Test Information Provides information that may help with selection of the correct test or proper submission of the test request

See Targeted Genes Interrogated by NGCDA Next-Generation Sequencing in Special Instructions for a list of the genes and exons targeted by this test.

Special Instructions and Forms Describes specimen collection and preparation information, test algorithms, and other information pertinent to test. Also includes pertinent information and consent forms to be used when requesting a particular test

Method Name A short description of the method used to perform the test

Hereditary Mutation Detection by Next-Generation Sequencing (NGS)

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Conditional

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

CDA Sequencing, V

Aliases Lists additional common names for a test, as an aid in searching

CDA
CDA type I
CDA type II
CDA type III
CDA type IV
C15ORF41
CDAN1
GATA1
KIF23
KLF1
SEC23B
Congenital dyserythropoietic anemia type I
Congenital dyserythropoietic anemia type Il
Congenital dyserythropoietic anemia type lll
Congenital dyserythropoietic anemia type IV