Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

10 matching diseasesClear search ×

Sickle cell anemia

Homozygous hemoglobin S · Homozygous sickle cell anemia SS

ORPHA:232

Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome

HbSS disease · HPFH-sickle cell disease syndrome

ORPHA:251380

Sickle cell disease

HbSS disease · SCD

ORPHA:275752

Sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variant

HbSS disease · SCD

ORPHA:700085

Sickle cell S-C disease

Hemoglobin S-C disease · HbSC disease

ORPHA:251365

Sickle cell S-E disease

HbSE disease · Hemoglobin S-E disease

ORPHA:251375

Sickle cell S-O Arab disease

Hemoglobin S-O Arab disease · HbS-O Arab disease

ORPHA:700090

Sickle cell-beta plus-thalassemia

HbS-beta plus-thalassemia · HbS-beta+ thalassemia

ORPHA:695147

Sickle cell-beta zero-thalassemia

HbS-beta0 thalassemia · HbS-beta zero-thalassemia

ORPHA:695140

Sickle cell-beta-thalassemia disease

HbS-beta-thalassemia syndrome

ORPHA:251359