Mendelian Genetic Inheritance for SCD
Sickle Cell Disease is an autosomal recessive condition. A child inherits one hemoglobin gene from each parent.
| Parent 1 Genotype | Parent 2 Genotype | AA (Normal) % | AS (Trait) % | SS (Disease) % |
|---|---|---|---|---|
| AA | AA | 100% | 0% | 0% |
| AA | AS | 50% | 50% | 0% |
| AA | SS | 0% | 100% | 0% |
| AS | AS | 25% | 50% | 25% |
| AS | SS | 0% | 50% | 50% |
| SS | SS | 0% | 0% | 100% |
Key Medical Definitions
- Genotype AA: Normal hemoglobin. Healthy non-carrier.
- Genotype AS: Sickle Cell Trait. Generally asymptomatic carrier.
- Genotype SS: Sickle Cell Disease (Anemia). Symptomatic condition requiring management.