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3A51.1 Sickle cell disease without crisis

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

A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing.

synonyms

• Sickle cell disease without crisis
• Hb-SS disease without crisis
• HbSS without crisis
• Sickle-cell anaemia without crisis
• SCD - [sickle cell disease]
• SCA - [sickle cell anaemia]
• sickle cell disease NOS
• sickle cell disorder
• sickle cell syndrome
• Sickle-cell anaemia NOS
• sickle-cell disorder NOS
• haemoglobin S disease
• haemoglobin SS disease
• Hb S disease
• Hb SS disease
• Herrick anaemia
• hereditary haemoglobinopathy disorder homozygous for haemoglobin S
• sickle-cell haemoglobin disease
• sickling disorder due to haemoglobin S
• Sickle cell nephropathy
• Drepanocythemia
• drepanocytic anaemia
• drepanocytosis

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