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Congenital dyserythropoietic anemia type II

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Name:
Congenital dyserythropoietic anemia type II
Description:
Congenital dyserythropoietic anemia type II (CDA II) is the most common form of CDA (see this term) characterized by anemia, jaundice and splenomegaly and often leading to liver iron overload and gallstones.
ORPHAcode:
98873
Synonyms:
CDA II
CDA type 2
CDA type II
Congenital dyserythropoietic anemia type 2
Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)
SEC23B-CDG
XREF(s):
Orphanet
OMIM
ICD-10
Analyte(s):
SEC23B
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14
  • Hemochromatosis (17 genes) - ULB
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    ALAS2 100.00 1 NM_000032
    CDAN1 100.00 1 NM_138477
    CP 100.00 1 NM_000096
    FTH1 100.00 1 NM_002032
    FTL 100.00 1 NM_000146
    HAMP 100.00 1 Core gene / NM_021175
    HFE1 100.00 1 NM_000410
    HJV 100.00 1 Core gene / NM_213653
    HMOX1 100.00 1 NM_002133
    SEC23B 100.00 1 NM_006363
    SLC11A2 100.00 1 Core gene / NM_000617
    SLC25A38 100.00 1 NM_017875
    SLC40A1 100.00 1 NM_014585
    STEAP3 100.00 1 NM_001008410
    TF 100.00 1 NM_001063
    TFR2 100.00 1 Core gene / NM_003227
    TMPRSS6 100.00 1 NM_153609