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Disease Anemia, Dyserythropoietic, Congenital

Name Anemia, Dyserythropoietic, Congenital
Synonyms Anemia, Congenital Dyserythropoietic | ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I | ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia | Anemia, Congenital Dyserythropoietic, Type II | ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE III | ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IV | Anemia, Dyserythropoietic, Congenital Type 1 | Anemia, Dyserythropoietic, Congenital Type 2 | Anemia, Dyserythropoietic Congenital, Type I | Anemia, Dyserythropoietic, Congenital, Type I | Anemia, Dyserythropoietic Congenital, Type II | Anemia, Dyserythropoietic, Congenital, Type II | Anemia, Dyserythropoietic Congenital, Type III | Anemia, Dyserythropoietic, Congenital, Type III | Anemias, Congenital Dyserythropoietic | Anemia With Multinucleated Erythroblasts | CDA Ia | CDA II | CDA III | CDAN1A | CDAN2 | CDAN3 | CDAN4 | CDA, TYPE IV | Congenital Dyserythropoietic Anemia | Congenital Dyserythropoietic Anemias | Congenital Dyserythropoietic Anemia Type 1 | Congenital Dyserythropoietic Anemia, Type I | Congenital Dyserythropoietic Anemia Type II | Congenital Dyserythropoietic Anemia, Type III | Dyserythropoietic Anemia, Congenital | Dyserythropoietic Anemia, Congenital Type 1 | Dyserythropoietic Anemia, Congenital Type 2 | Dyserythropoietic Anemia, Congenital, Type I | DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia | Dyserythropoietic Anemia, Congenital, Type II | Dyserythropoietic Anemia, Congenital, Type III | Dyserythropoietic Anemia, HEMPAS Type | Dyserythropoietic Anemias, Congenital | ERYTHRORETICULOSIS, HEREDITARY BENIGN | HEMPAS | HEMPAS Anemia | HEMPAS Anemias | Hereditary Erythroblastic Multinuclearity with Positive Acidified-Serum Test | Hereditary Erythroblast Multinuclearity with Positive Acidified Serum | Type I Congenital Dyserythropoietic Anemia
Definition A familial disorder characterized by ANEMIA with multinuclear ERYTHROBLASTS, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors (ERYTHROID PRECURSOR CELLS). Type II is the most common of the 3 types; it is often referred to as HEMPAS, based on the Hereditary Erythroblast Multinuclearity with Positive Acidified Serum test.
Categories Blood disease | Genetic disease (inborn)
MeSH® ID D000742
OMIM® IDs 105600 | 224100 | 224120 | 613673
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Top ↑ Ancestors

1. DiseasesHemic and Lymphatic Diseases Has associated chemicals Has associated genes Has associated exposure references Hematologic Diseases Has associated chemicals Has associated genes Has associated exposure references Anemia Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic, Congenital Has associated chemicals Has associated genes Has associated exposure references Anemia, Dyserythropoietic, Congenital Has associated chemicals Has associated genes
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic, Congenital Has associated chemicals Has associated genes Has associated exposure references Anemia, Dyserythropoietic, Congenital Has associated chemicals Has associated genes

Top ↑ Descendants

Anemia, Dyserythropoietic, Congenital Has associated chemicals Has associated genes
  Dyserythropoietic Anemia with Thrombocytopenia
  Erythroreticulosis, Hereditary Benign
  Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis Has associated chemicals Has associated genes
  Majeed syndrome Has associated chemicals Has associated genes
  THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Has associated chemicals Has associated genes