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Sickle cell - hemoglobin E disease

1 associated gene
No signs/symptoms info

COMMON GENES: 1

Beta-thalassemia intermedia

1 OMIM reference -
1 associated gene
12 signs/symptoms

Sickle cell - hemoglobin E disease

Beta-thalassemia intermedia

HBB

(UniProt - OMIM)

HBB

(UniProt - OMIM)


COMMON GENES	HBB

Citations in the biomedical literature:

Sickle cell - hemoglobin E disease		Beta-thalassemia intermedia
	Synonym(s): - HbSE disease		Synonym(s): (no synonyms)

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

Beta-thalassemia intermedia
	Very frequent - Anaemia - Anomalies of bones / skeletal anomalies - Hemoglobinosis / hemoglobinopathy - Microcytic anemia - 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
Sickle cell - hemoglobin E disease
(no data available)