ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Acute myeloblastic leukemia without maturation

X-linked Opitz G/BBB syndrome

FLT3	(UniProt - OMIM)		MID1	(UniProt - OMIM)
NPM1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NPM1	(0.63)	MID1

Citations in the biomedical literature:

Acute myeloblastic leukemia without maturation		X-linked Opitz G/BBB syndrome
	Synonym(s): - Acute myeloblastic leukemia type 1		Synonym(s): - X-linked Opitz BBB/G syndrome - X-linked Opitz syndrome - XLOS

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare urogenital disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

No signs/symptoms info available.