Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.
  • page settings
  • hide sidebar
  • show empty fields
  • layout
  • (too narrow)
  • open all
  • close all
Resources » Disease Ontology

congenital dyserythropoietic anemia type Ia

  • Ontology Browser

  • Tree Display

  • My Favorites

  • My Library

  • Comments on congenital dyserythropoietic anemia type Ia (0)

  • Overview

    congenital dyserythropoietic anemia type Ia

    Ontology Term:
    Status:
    Live
    Synonym:
    CDA Ia
    CDAN1A
    Type:
    Mapping to OMIM ID:
    Comparative Info:
    Learn more about this disease from studies in other model systems at the
    WormBase ID:
    DOID:0111398
    A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in the CDAN1 gene on chromosome 15q15.2.
    Child:
    Associations based on experimental data:
    Disease relevant gene:
    Automatic gene association:
    1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation