ODCs

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

PROTEIN INTERACTIONS: 1

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

Combined pituitary hormone deficiencies, genetic forms

Acute myeloid leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POU1F1	(0.88)	GATA2

Citations in the biomedical literature:

Combined pituitary hormone deficiencies, genetic forms		Acute myeloid leukemia
	Synonym(s): - Familial congenital hypopituitarism - Multiple pituitary hormone deficiencies, genetic forms		Synonym(s): - AML - Acute myelogenous leukemia - Acute non-lymphoblastic leukemia

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility		Classification (Orphanet): (no data available)

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

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

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D015470

No signs/symptoms info available.