3A51.3
Compound heterozygous sickling disorders without crisis
Transtornos falciformes heterozigotos compostos sem crise
CategoryDefinition
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.
Inclusions
- Sickle cell Hb-C disease without crisis
- Sickle cell thalassaemia without crisis
Index Terms
Compound heterozygous sickling disorders without crisisdouble heterozygous sickling disorderSickle cell Hb-C disease without crisisHb SC diseaseHb S Hb C diseasesickle-cell HbC diseaseSickle cell thalassaemia without crisissickle-cell thalassaemiasickle-cell beta thalassaemiahaemoglobin s/beta thalassaemiathalassaemia with haemoglobin S diseasemicrodrepanocytosisdouble heterozygous for Hb S or beta thalassaemiaCompound HbS or HbC heterozygotesCompound HbS, HbD-Punjab or Los Angeles heterozygotesHb-SD diseaseCompound HbS or HbE heterozygotesHb SE diseaseCompound HbS or O-Arab heterozygotesDouble heterozygous sickling disorders with retinopathyGlomerular disorders in double heterozygous sickling disordersGouty arthropathy in double heterozygous sickling disordersCompound HbS or beta thalassaemia heterozygotesCompound HbS and beta thalassaemia heterozygotes including HbS/delta-beta-thal compoundsHereditary persistence of fetal haemoglobin - sickle cell disease