About
Although these conditions do not tend to cause health problems, consultation with a Pediatric Hematologist is recommended.
Hemoglobin C Disease
Affects 2-3% of the African American population in the United States. Usually does not cause health problems other than a low blood count or anemia. The anemia that develops is mild. However, some may develop infections, enlarged spleen, increased risk for gallstones, episodes of joint pain, and increased risk of infection.
Hemoglobin D Disease
This is most common among people of India, Pakistan, England, Ireland, Holland, Australia, China, Iran and Turkey ancestry. It is rare and a relatively mild disease. However, some people develop an enlarged spleen and may need treatment at the time.
Hemoglobin E Disease
This is common in people of Southeast Asian ancestry. Usually does not cause health problems other than anemia and a low blood count and requires no treatment, some people may develop an enlarged spleen.
Condition Type:
Secondary
Frequency:
More Information for Parents:
Also known as:
- Hemoglobin C Disease
- Hemoglobin D Disease
- Hemoglobin E Disease
- FC, FD, FE
- Alternative Name 5
Core Conditions
- Propionic Acidemia (PROP)
- Methylmalonic Acidemia (Methylmalonyl-CoA Mutase Deficiency) (MUT)
- Methylmalonic Acidemia (Cobalamin Conditions)
- Isovaleric Acidemia (IVA)
- 3-Methylcrotonyl-CoA Carboxylase Deficiency (3-MCC)
- 3-Hydroxy-3-Methylglutaric Aciduria (HMG)
- Holocarboxylase Synthetase Deficiency (MCD)
- Beta-Ketothiolase Deficiency (BKT)
- Glutaric Acidemia, Type I (GA-1)
- Mucopolysaccharidosis, Type II (MPS II)
- Biotinidase Deficiency (BIOT)
- Critical Congenital Heart Disease (CCHD)
- Cystic Fibrosis (CF)
- Classic Galactosemia (GALT)
- Hearing Loss or Varying Hearing Levels
- Severe Combined Immunodeficiency (SCID)
- X-Linked Adrenoleukodystrophy (X-ALD)
- Pompe
- Spinal Muscular Atrophy (SMA)
- Mucopolysaccharidosis, Type I (MPS I)
Secondary
- Citrullinemia, Type II (CIT II)
- Hypermethioninemia (MET)
- Benign Hyperphenylalaninemia (H-PHE)
- Biopterin Defect in Cofactor Biosynthesis (BIOPT-BS)
- Biopterin Defect in Cofactor Regeneration (BIOPT-REG)
- Ornithine Transcarbamylase Deficiency (OTC)
- Carbamoyl Phosphate Synthetase Deficiency (CPS)
- Tyrosinemia, Type II (TYR II)
- Tyrosinemia, Type III (TYR III)