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1 OMIM reference -
1 associated gene
13 signs/symptoms

PROTEIN INTERACTIONS: 2

Acute myeloid leukemia with t(8;21)(q22;q22) translocation

5 associated genes
No signs/symptoms info

Cherubism

Acute myeloid leukemia with t(8;21)(q22;q22) translocation

SH3BP2	(UniProt - OMIM)		CEBPA	(UniProt - OMIM)
			FLT3	(UniProt - OMIM)
			KIT	(UniProt - OMIM)
			RUNX1	(UniProt - OMIM)
			RUNX1T1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SH3BP2 SH3BP2	(0.72) (0.63)	KIT FLT3

Citations in the biomedical literature:

Cherubism		Acute myeloid leukemia with t(8;21)(q22;q22) translocation
	Synonym(s): - CRBM		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare odontologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the digestive system -		Classification (ICD10): - Neoplasms -

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

	External references: 1 OMIM reference - 1 MeSH reference: D002636		External references: No OMIM references No MeSH references

Cherubism
	Very frequent - Autosomal dominant inheritance - Bone / osseous neoplasm / tumor / carcinoma / cancer - Enlargment of jaw / large jaw - High cheek bones Frequent - Abnormal dentition / dental position / implantation / unerupted / dental ankylosis - Anodontia / oligodontia / hypodontia - Tooth shape anomaly Occasional - Abnormal cry / voice / phonation disorder / nasal speech - Apnea / sleep apnea - Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Proptosis / exophthalmos - Visual loss / blindness / amblyopia
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
(no data available)