ODCs

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

PROTEIN INTERACTIONS: 1

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

Familial expansile osteolysis

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TNFRSF11A	(0.55)	CBL

Citations in the biomedical literature:

Familial expansile osteolysis		Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
	Synonym(s): - Hereditary expansile polyostotic osteolytic dysplasia - McCabe's disease		Synonym(s): - CBL syndrome - Noonan syndrome-like disorder with JMML

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

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

	External references: 1 OMIM reference - 1 MeSH reference: C536335		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.