Anemia, Congenital Dyserythropoietic, Type Ia (CDAN1A)

Alias:

Congenital Dyserythropoietic Anemia Type I

Cda I

Congenital Dyserythropoietic Anemia Type Ia

Congenital Dyserythropoietic Anemia, Type I

Congenital Dyserythropoietic Anemia Type 1

Cda Type 1

Cda Type I

Cdan1a

Anemia, Congenital Dyserythropoietic, Type 1a

Anemia, Congenital Dyserythropoietic, Type I

Cda Ia

Anemia, Dyserythropoietic, Congenital, Type Ia

Dyserythropoietic Anemia, Congenital, Type Ia

Congenital Dyserythropoietic Anaemia Type 1

Congenital Dyserythropoietic Anaemia Type I

Dyserythropoietic Anemia, Congenital Type 1

Anemia, Congenital Dyserythropoietic, 1a

Cda, Type Ia

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Anemia, Congenital Dyserythropoietic, Type Ia, also known as congenital dyserythropoietic anemia type i, is related to anemia, congenital dyserythropoietic, type ib and congenital dyserythropoietic anemia, and has symptoms including icterus An important gene associated with Anemia, Congenital Dyserythropoietic, Type Ia is CDAN1 (Codanin 1), and among its related pathways/superpathways are SARS-CoV-2 Infection and Response to elevated platelet cytosolic Ca2+. The drugs Omeprazole and Iron have been mentioned in the context of this disorder. Affiliated tissues include bone and liver, and related phenotypes are syndactyly and hepatomegaly

Related ID：

MALACARDS：ANM043

OMIM：224120

MESH：D000742