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Delta-beta-thalassemia

1 OMIM reference -
3 associated genes
3 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 3

Beta-thalassemia intermedia

1 OMIM reference -
1 associated gene
12 signs/symptoms

Delta-beta-thalassemia

Beta-thalassemia intermedia

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


COMMON GENES	HBB

Citations in the biomedical literature:

Delta-beta-thalassemia		Beta-thalassemia intermedia

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

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


COMMON SIGNS	- Anaemia - Hemoglobinosis / hemoglobinopathy - Microcytic anemia

Delta-beta-thalassemia		Beta-thalassemia intermedia
	(no more signs)		Very frequent - Anomalies of bones / skeletal anomalies - Splenomegaly Frequent - Biliary / gallbladder stones / lithiasis / cholecystitis - Hepatomegaly / liver enlargement (excluding storage disease) - Hyperferritinemia / iron overload Occasional - Chronic skin infection / ulcerations / ulcers / cancrum - Hepatic / liver neoplasm / tumor / carcinoma / cancer - Pulmonary hypertension - Venous thrombosis / phlebitis / thrombophlebitis