ODCs

Click node...

11 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Familial cerebral saccular aneurysm

Multiple keratoacanthoma, Ferguson-Smith type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ENG	(0.95)	TGFBR1

Citations in the biomedical literature:

Familial cerebral saccular aneurysm		Multiple keratoacanthoma, Ferguson-Smith type
	Synonym(s): - Familial berry aneurysm - Familial intracranial saccular aneurysm		Synonym(s): - ESS1 - MSSE - Multiple self-healing squamous epithelioma - Self-healing squamous epithelioma type 1

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: - 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: normal Type of inheritance: autosomal dominant

	External references: 11 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.