| D58.0 |
Hereditary spherocytosis
Acholuric (familial) jaundice
Congenital (spherocytic) haemolytic icterus
Minkowski-Chauffard syndrome
|
| D58.1 |
Hereditary elliptocytosis
Elliptocytosis (congenital)
Ovalocytosis (congenital)(hereditary)
|
| D58.2 |
Other haemoglobinopathies
Abnormal haemoglobin NOS
Congenital Heinz body anaemia
Disease:
· Hb-C
· Hb-D
· Hb-E
Haemoglobinopathy NOS
Unstable haemoglobin haemolytic disease
Excludes:
- familial polycythaemia ( D75.0 )
- Hb-M disease ( D74.0 )
- hereditary persistence of fetal haemoglobin [HPFH] ( D56.4 )
- high-altitude polycythaemia ( D75.1 )
- methaemoglobinaemia ( D74.- )
|
| D58.8 |
Other specified hereditary haemolytic anaemias
Stomatocytosis
|
| D58.9 |
Hereditary haemolytic anaemia, unspecified
|