Disease #00165 (SCD (Sickle Cell Anemia), OMIM:603903)

Official abbreviation SCD
Name Sickle Cell Anemia
OMIM ID 603903
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene HBB
Associated tissues -
Disease features -
Remarks -


Individuals

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00001047 Lie-Injo et al - Malaysia India - - - SCD Hb S trait carriers HBB HBB 1 1 MyHVP Team
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