Congenital Dyserythropoietic Anemia (CDA)

Alias:
Cda
Congenital Dyshaematopoietic Anaemia
Dyserythropoietic Dyshaematopoietic Congenital Anaemia
Cda - [congenital Dyserythropoietic Anaemia]
Anemia, Dyserythropoietic, Congenital
Dyserythropoietic Anemia, Congenital
Anemia Dyserythropoietic Congenital
Dyshaematopoietic Anaemia
Dyserythropoietic Anaemia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Dyserythropoietic Anemia, also known as cda, is related to anemia, congenital dyserythropoietic, type ia and anemia, congenital dyserythropoietic, type iiia. An important gene associated with Congenital Dyserythropoietic Anemia is SEC23B (SEC23 Homolog B, COPII Coat Complex Component), and among its related pathways/superpathways are Response to elevated platelet cytosolic Ca2+ and Cell surface interactions at the vascular wall. The drugs Omeprazole and Iron have been mentioned in the context of this disorder. Affiliated tissues include liver and heart, and related phenotypes are Decreased viability and homeostasis/metabolism
Related ID:
MESH:D000742
ICD11:899830967

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLD
AD
AR
XL
Child
1-9/1000000
25
207
--

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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