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3A70.0 Congenital aplastic anaemia

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

inclusions

• familial hypoplastic anaemia
• Constitutional medullar aplasia
• Fanconi anaemia

exclusions

• Congenital amegakaryocytic thrombocytopenia  (3B64.01)

code elsewhere

• Congenital hypoplastic anaemia  (KA8C)
• Noonan syndrome  (LD2F.15)

synonyms

• Congenital aplastic anaemia
• constitutional aplastic anaemia
• congenital or familial hypoplastic anaemia
• congenital pancytopenia
• constitutional aplastic anaemia with malformation
• Constitutional medullar aplasia
• familial hypoplastic anaemia
• constitutional panhemocytopenia
• constitutional panhaematopenia
• pancytopenia with malformation
• Fanconi anaemia
• Fanconi pancytopenia
• Fanconi pancytopenia syndrome
• Fanconi-ichthyosis-dysmorphism syndrome
• Fanconi familial refractory anaemia
• Fanconi hypoplastic anaemia
• Dyskeratosis congenita
• Autosomal dominant dyskeratosis congenita
• AD-DKC - [Autosomal dominant dyskeratosis congenita]
• Autosomal recessive dyskeratosis congenita
• AR-DKC - [Autosomal recessive dyskeratosis congenita]
• Hoyeraal-Hreidarsson syndrome
• Progressive pancytopenia - immunodeficiency - cerebellar hypoplasia
• Shwachman-Diamond syndrome
• Congenital lipomatosis of pancreas
• WT limb-blood syndrome

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