ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

1 OMIM reference -
2 associated genes
No signs/symptoms info

Hemoglobin H disease

Juvenile polyposis of infancy

HBA1	(UniProt - OMIM)		BMPR1A	(UniProt - OMIM)
HBA2	(UniProt - OMIM)		PTEN	(UniProt - OMIM)


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

Citations in the biomedical literature:

Hemoglobin H disease		Juvenile polyposis of infancy
	Synonym(s): - Alpha-thalassemia intermedia - HbH disease		Synonym(s): - Infantile juvenile polyposis syndrome

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare hematologic disease - Rare renal disease		Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic 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: 1-9 / 1 000 000 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: before age 5 Type of inheritance: autosomal dominant

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

No signs/symptoms info available.