ODCs

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1 OMIM reference -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

4 OMIM references -
1 associated gene
2 signs/symptoms

Juvenile myelomonocytic leukemia

Hereditary gingival fibromatosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PTPN11 CBL	(0.83) (0.63)	SOS1 SOS1

Citations in the biomedical literature:

Juvenile myelomonocytic leukemia		Hereditary gingival fibromatosis
	Synonym(s): - Juvenile chronic myelomonocytic leukemia		Synonym(s): - Autosomal dominant gingival fibromatosis - Autosomal dominant gingival hyperplasia - Hereditary gingival hyperplasia

	Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare odontologic disease

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

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

	External references: 1 OMIM reference - 1 MeSH reference: D054429		External references: 4 OMIM references - No MeSH references

Hereditary gingival fibromatosis
	Very frequent - Autosomal dominant inheritance - Thickened / hypertrophic / fibromatous gingivae
Juvenile myelomonocytic leukemia
(no data available)