ODCs

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1 OMIM reference -
3 associated genes
3 signs/symptoms

PROTEIN INTERACTIONS: 2

1 OMIM reference -
1 associated gene
No signs/symptoms info

Delta-beta-thalassemia

Hereditary cerebral hemorrhage with amyloidosis, Flemish type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBD HBG1	(0.56) (0.56)	APP APP

Citations in the biomedical literature:

Delta-beta-thalassemia		Hereditary cerebral hemorrhage with amyloidosis, Flemish type
	Synonym(s): (no synonyms)		Synonym(s): - HCHWA, Flemish type

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

Delta-beta-thalassemia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Microcytic anemia
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
(no data available)