ODCs

Click node...

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

PROTEIN INTERACTIONS: 2

1 associated gene
No signs/symptoms info

Familial multiple meningioma

Glucocorticoid resistance


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SMARCE1 SMARCB1	(0.74) (0.55)	NR3C1 NR3C1

Citations in the biomedical literature:

Familial multiple meningioma		Glucocorticoid resistance

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare urogenital disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.