Anemia, Congenital Dyserythropoietic, Type Ii (CDAN2)

Alias:

Congenital Dyserythropoietic Anemia Type Ii

Cda Ii

Hereditary Erythroblastic Multinuclearity with a Positive Acidified-Serum Test

Congenital Dyserythropoietic Anemia, Type Ii

Congenital Dyserythropoietic Anemia Type 2

Cda Type Ii

Cda Type 2

Sec23b-Cdg

Cdan2

Hereditary Erythroblastic Multinuclearity with Positive Acidified-Serum Test

Hempas

Anemia, Dyserythropoietic, Congenital, Type Ii

Dyserythropoietic Anemia, Congenital, Type Ii

Anemia, Dyserythropoietic Congenital, Type Ii

Congenital Dyserythropoietic Anaemia Type Ii

Congenital Dyserythropoietic Anaemia Type 2

Dyserythropoietic Anemia, Congenital Type 2

Anemia, Congenital Dyserythropoietic, 2

Dyserythropoietic Anemia, Hempas Type

Dyserythropoietic Anemia Hempas Type

Cda, Type Ii

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Anemia, Congenital Dyserythropoietic, Type Ii, also known as congenital dyserythropoietic anemia type ii, is related to cowden syndrome 7 and congenital dyserythropoietic anemia, and has symptoms including icterus An important gene associated with Anemia, Congenital Dyserythropoietic, Type Ii is SEC23B (SEC23 Homolog B, COPII Coat Complex Component), and among its related pathways/superpathways are Metabolism of proteins and Class I MHC mediated antigen processing and presentation. Affiliated tissues include bone marrow and liver, and related phenotypes are reticulocytosis and splenomegaly

Related ID：

MALACARDS：ANM042

OMIM：224100

MESH：D000742