ODCs

Click node...

4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Hereditary persistence of fetal hemoglobin - sickle cell disease

Familial isolated congenital asplenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBG2	(0.63)	RPSA

Citations in the biomedical literature:

Hereditary persistence of fetal hemoglobin - sickle cell disease		Familial isolated congenital asplenia
	Synonym(s): - HPFH - sickle cell disease		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: - Average age onset: - 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.