ODCs

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3 OMIM references -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Homozygous familial hypercholesterolemia

Acute myeloid leukemia with t(8;16)(p11;p13) translocation


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LDLR	(0.52)	CREBBP

Citations in the biomedical literature:

Homozygous familial hypercholesterolemia		Acute myeloid leukemia with t(8;16)(p11;p13) translocation
	Synonym(s): - HoFH		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.