ODCs

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

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

X-linked Opitz G/BBB syndrome

Acute myelomonocytic leukemia

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


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

Citations in the biomedical literature:

X-linked Opitz G/BBB syndrome		Acute myelomonocytic leukemia
	Synonym(s): - X-linked Opitz BBB/G syndrome - X-linked Opitz syndrome - XLOS		Synonym(s): (no synonyms)

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

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

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

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: D015479

No signs/symptoms info available.