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Delta-beta-thalassemia

1 OMIM reference -
3 associated genes
3 signs/symptoms

COMMON GENES: 1

Hemoglobin C disease

1 associated gene
No signs/symptoms info

Delta-beta-thalassemia

Hemoglobin C disease

HBB	(UniProt - OMIM)		HBB	(UniProt - OMIM)
HBD	(UniProt - OMIM)
HBG1	(UniProt - OMIM)


COMMON GENES	HBB

Citations in the biomedical literature:

Delta-beta-thalassemia		Hemoglobin C disease

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic 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: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: D006445

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