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Delta-beta-thalassemia

1 OMIM reference -
3 associated genes
3 signs/symptoms

COMMON GENES: 1
PROTEIN INTERACTIONS: 4

Autosomal dominant methemoglobinemia

3 associated genes
No signs/symptoms info

Delta-beta-thalassemia

Autosomal dominant methemoglobinemia

HBB	(UniProt - OMIM)		HBA1	(UniProt - OMIM)
HBD	(UniProt - OMIM)		HBA2	(UniProt - OMIM)
HBG1	(UniProt - OMIM)		HBB	(UniProt - OMIM)


COMMON GENES	HBB


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBB HBB HBD HBD	(0.96) (0.96) (0.63) (0.63)	HBA1 HBA2 HBA1 HBA2

Citations in the biomedical literature:

Delta-beta-thalassemia		Autosomal dominant methemoglobinemia
	Synonym(s): (no synonyms)		Synonym(s): - Hemoglobin M disease - Hereditary methemoglobinemia due to hemoglobin mutation - M hemoglobinopathy

	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: - Average age of death: - Type of inheritance: autosomal dominant

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

Delta-beta-thalassemia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Microcytic anemia
Autosomal dominant methemoglobinemia
(no data available)