3A51.3Compound heterozygous sickling disorders without crisis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed
synonyms
Compound heterozygous sickling disorders without crisis
double heterozygous sickling disorder
Sickle cell Hb-C disease without crisis
Hb SC disease
Hb S Hb C disease
sickle-cell HbC disease
Sickle cell thalassaemia without crisis
sickle-cell thalassaemia
sickle-cell beta thalassaemia
haemoglobin s/beta thalassaemia
thalassaemia with haemoglobin S disease
microdrepanocytosis
double heterozygous for Hb S or beta thalassaemia
Compound HbS or HbC heterozygotes
Compound HbS, HbD-Punjab or Los Angeles heterozygotes
Hb-SD disease
Compound HbS or HbE heterozygotes
Hb SE disease
Compound HbS or O-Arab heterozygotes
Double heterozygous sickling disorders with retinopathy
Glomerular disorders in double heterozygous sickling disorders
Gouty arthropathy in double heterozygous sickling disorders
Compound HbS or beta thalassaemia heterozygotes
Compound HbS and beta thalassaemia heterozygotes including HbS/delta-beta-thal compounds
Hereditary persistence of fetal haemoglobin - sickle cell disease