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

Synpolydactyly type 1

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

HOXD13	(UniProt - OMIM)		CREBBP	(UniProt - OMIM)
			KAT6A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HOXD13	(0.56)	CREBBP

Citations in the biomedical literature:

Synpolydactyly type 1		Acute myeloid leukemia with t(8;16)(p11;p13) translocation
	Synonym(s): - SD2, Vordingborg type - SD2a - SPD, Vordingborg type - SPD1 - Synpolydactyly, Vordingborg type		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic 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 No MeSH references

No signs/symptoms info available.