ODCs

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4 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 2

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

Hereditary persistence of fetal hemoglobin - sickle cell disease

Hemoglobinopathy Toms River


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBB HBG1	(0.52) (0.49)	HBG2 HBG2

Citations in the biomedical literature:

Hereditary persistence of fetal hemoglobin - sickle cell disease		Hemoglobinopathy Toms River
	Synonym(s): - HPFH - sickle cell disease		Synonym(s): - Transient neonatal cyanosis and anemia due to Toms River Hemoglobin

	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: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.