3A10.Y Other specified hereditary haemolytic anaemia

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

synonyms

• Other specified hereditary haemolytic anaemia
• Hereditary haemolytic anaemia due to enzyme deficiency
• Constitutional haemolytic anaemia due to enzyme deficiency
• anaemia due to enzyme disorders
• Haemolytic anaemias due to disorders of glycolytic enzymes
• anaemia due to disorders of glycolytic enzymes
• anaemia due to anaerobic glycolysis disorder
• anaemia due to glycolytic enzyme deficiency
• glycolysis anaerobic disorder with anaemia
• Haemolytic anaemia due to triose phosphate-isomerase deficiency
• Haemolytic anaemia due to red cell pyruvate kinase deficiency
• pyruvate kinase deficiency anaemia
• hereditary nonspherocytic haemolytic anaemia due to pyruvate kinase deficiency
• Haemolytic anaemia due to glucose-phosphate isomerase deficiency
• Haemolytic anaemia due to glucophosphate isomerase deficiency
• Haemolytic anaemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
• anaemia due to glyceraldehyde phosphate dehydrogenase deficiency
• Haemolytic anaemia due to red cell enolase deficiency
• Erythrocyte enolase deficiency
• Haemolytic anaemia due to red cell diphosphoglycerate mutase deficiency
• Nonspherocytic haemolytic anaemia due to hexokinase deficiency
• anaemia due to hexokinase deficiency
• Haemolytic nonspherocytic hereditary anaemia, type 2
• haemolytic nonspherocytic anaemia, type 2
• Haemolytic anaemias due to disorders of nucleotide metabolism
• anaemia due to disorders of nucleotide metabolism
• Haemolytic anaemia due to adenosine triphosphatase deficiency
• Haemolytic anaemia due to pyrimidine 5' nucleotidase deficiency
• Uridine monophosphate hydrolase deficiency
• Haemolytic anaemia due to adenylate kinase deficiency
• Hereditary haemolytic anaemia due to red cell membrane defects
• Constitutional haemolytic anaemia due to red cell membrane defects
• Hereditary spherocytosis
• Minkowski-Chauffard disease
• Acholuric (familial) jaundice
• congenital spherocytosis
• familial spherocytosis
• Minkowski-Chauffard syndrome
• anaemia spherocytic
• acholuric icterus
• acholuric jaundice
• congenital haemolytic icterus
• Congenital (spherocytic) haemolytic icterus
• hereditary spherocytic anaemia
• spherocytosis
• congenital spherocytic haemolytic anaemia
• Southeast Asian ovalocytosis
• Hereditary stomatocytosis
• Dehydrated hereditary stomatocytosis
• Xerocytosis
• Hereditary cryohydrocytosis with reduced stomatin
• Hereditary cryohydrocytosis
• Intermediate stomatocytosis syndrome
• Overhydrated hereditary stomatocytosis
• Hydrocytosis
• Rh deficiency syndrome
• Rh-null syndrome
• Acanthocytosis
• Choreoacanthocytosis
• Neuroacanthocytosis
• McLeod neuroacanthocytosis syndrome
• Hereditary haemolytic uraemic syndrome
• Atypical haemolytic uraemic syndrome
• Constitutional haemolytic uraemic syndrome
• Haemolytic-uremic syndrome without diarrhoea
• Atypical haemolytic uraemic syndrome with C3 anomaly
• Atypical haemolytic uraemic syndrome with MCP or CD46 anomaly
• Atypical haemolytic uraemic syndrome with factor B anomaly
• Atypical haemolytic uraemic syndrome with factor H anomaly
• Atypical haemolytic uraemic syndrome with factor I anomaly
• Atypical haemolytic uraemic syndrome with thrombomodulin anomaly

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