3A70.0
Congenital aplastic anaemia
Anemia aplástica congênita
CategoryDefinition
A disease caused by determinants in the antenatal period leading to the inability of stem cells to generate new mature cells. This disease is characterised by low levels of red blood cells, white blood cells, platelets. This disease may present with pallor, fatigue, dizziness, increased risk of infection or increased bruising or bleeding.
Exclusions
- Congenital amegakaryocytic thrombocytopenia
Inclusions
- familial hypoplastic anaemia
- Constitutional medullar aplasia
- Fanconi anaemia
Index Terms
Congenital aplastic anaemiaconstitutional aplastic anaemiacongenital or familial hypoplastic anaemiacongenital pancytopeniaconstitutional aplastic anaemia with malformationConstitutional medullar aplasiafamilial hypoplastic anaemiaconstitutional panhemocytopeniaconstitutional panhaematopeniapancytopenia with malformationFanconi anaemiaFanconi pancytopeniaFanconi pancytopenia syndromeFanconi-ichthyosis-dysmorphism syndromeFanconi familial refractory anaemiaFanconi hypoplastic anaemiaDyskeratosis congenitaAutosomal dominant dyskeratosis congenitaAD-DKC - [Autosomal dominant dyskeratosis congenita]Autosomal recessive dyskeratosis congenitaAR-DKC - [Autosomal recessive dyskeratosis congenita]Hoyeraal-Hreidarsson syndromeProgressive pancytopenia - immunodeficiency - cerebellar hypoplasiaShwachman-Diamond syndromeCongenital lipomatosis of pancreasWT limb-blood syndrome