ODCs

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4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

2 OMIM references -
2 associated genes
No signs/symptoms info

Hereditary persistence of fetal hemoglobin - sickle cell disease

Familial rhabdoid tumor


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KLF1 KLF1	(0.85) (0.75)	SMARCB1 SMARCA4

Citations in the biomedical literature:

Hereditary persistence of fetal hemoglobin - sickle cell disease		Familial rhabdoid tumor
	Synonym(s): - HPFH - sickle cell disease		Synonym(s): - RTPS - Rhabdoid tumor predisposition syndrome

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - 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): (no data available)

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

	External references: No OMIM references No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.