Autosomal dominant aplasia and myelodysplasia

Orpha code: 314399OMIM code: 614675

Definition

A rare, genetic, hematologic disorder characterized by bone marrow failure which manifests with aplastic anemia and/or myelodysplasia, associated with hearing/ear abnormalities (such as deafness, labyrinthitis), inherited in an autosomal dominant manner.

Disease data
Classification

Disease

Synonyms
Autosomal dominant aplastic anemia and myelodysplasia
Autosomalna dominująca niedokrwistość aplastyczna i mielodysplazja
ORPHA code
314399
OMIM code
614675
ICD10 code
D61.0
ICD11 code
-

No additional description.

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