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Herpetic encephalitis

4 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Familial cylindromatosis

1 OMIM reference -
1 associated gene
5 signs/symptoms

Herpetic encephalitis

Familial cylindromatosis

TBK1	(UniProt - OMIM)		CYLD	(UniProt - OMIM)
TICAM1	(UniProt - OMIM)
TLR3	(UniProt - OMIM)
TRAF3	(UniProt - OMIM)
UNC93B1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TBK1	(0.76)	CYLD

Citations in the biomedical literature:

Herpetic encephalitis		Familial cylindromatosis
	Synonym(s): - HSV encephalitis - Herpes simplex encephalitis - Herpes simplex neuroinvasion		Synonym(s): - Turban tumor syndrome

	Classification (Orphanet): - Rare genetic disease - Rare immune disease - Rare infectious 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): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: any age Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536611

Familial cylindromatosis
	Very frequent - Autosomal dominant inheritance - Scalp cyst / giant nevus - Skin tumors / lumps / epidermal cysts - Subcutaneous nodules / lipomas / tumefaction / swelling - Telangiectasiae of the skin
Herpetic encephalitis
(no data available)