ODCs

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5 OMIM references -
5 associated genes
6 signs/symptoms

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Hereditary persistence of fetal hemoglobin - beta-thalassemia

Primary mediastinal large B-cell lymphoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	BCL11A	(0.84)	BCL6

Citations in the biomedical literature:

Hereditary persistence of fetal hemoglobin - beta-thalassemia		Primary mediastinal large B-cell lymphoma
	Synonym(s): - HPFH - beta-thalassemia		Synonym(s): - Large cell lymphoma of the mediastinum - Med-DLBCL - Mediastinal diffuse large-cell lymphoma with sclerosis - Primary mediastinal clear cell lymphoma of B-cell type

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 5 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

Hereditary persistence of fetal hemoglobin - beta-thalassemia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Pallor - Splenomegaly Frequent - Anomalies of bones / skeletal anomalies - Hepatomegaly / liver enlargement (excluding storage disease)
Primary mediastinal large B-cell lymphoma
(no data available)