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Hemoglobin C - beta-thalassemia

1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 2

Hemoglobin H disease

1 OMIM reference -
2 associated genes
No signs/symptoms info

Hemoglobin C - beta-thalassemia

Hemoglobin H disease

HBB	(UniProt - OMIM)		HBA1	(UniProt - OMIM)
			HBA2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBB HBB	(0.96) (0.96)	HBA1 HBA2

Citations in the biomedical literature:

Hemoglobin C - beta-thalassemia		Hemoglobin H disease
	Synonym(s): - C- beta-thalassemia - HbC - beta-thalassemia		Synonym(s): - Alpha-thalassemia intermedia - HbH disease

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare hematologic disease - Rare renal disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - No MeSH references

Hemoglobin C - beta-thalassemia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Microcytic anemia - Splenomegaly
Hemoglobin H disease
(no data available)