Catalog
Compound heterozygous sickling disorders without crisis
Link to WHO Definition
Compound heterozygous sickling disorders without crisis – http://id.who.int/icd/entity/313446364
A disease caused by genetic inheritance of two heterozygous recessive alleles of the haemoglobin gene leading to abnormal formation of haemoglobin molecule. This disease is characterised by rigid, sickle shaped red blood cells. Confirmation is by identification of mutations through genetic testing.
Parents
Children
- Gouty arthropathy in double heterozygous sickling disorders
- Compound HbS or O-Arab heterozygotes
- Compound HbS or HbE heterozygotes
- Sickle cell Hb-C disease without crisis
- Compound HbS or HbC heterozygotes
- Hereditary persistence of fetal haemoglobin - sickle cell disease
- Double heterozygous sickling disorders with retinopathy
- Compound HbS, HbD-Punjab or Los Angeles heterozygotes
- Compound HbS or beta thalassaemia heterozygotes
- Glomerular disorders in double heterozygous sickling disorders
- Sickle cell thalassaemia without crisis