ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Distal 17p13.3 microdeletion syndrome

Herpetic encephalitis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	YWHAE	(0.63)	TBK1

Citations in the biomedical literature:

Distal 17p13.3 microdeletion syndrome		Herpetic encephalitis
	Synonym(s): - Distal del(17)(p13.3 ) - Distal monosomy 17p13.3		Synonym(s): - HSV encephalitis - Herpes simplex encephalitis - Herpes simplex neuroinvasion

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare genetic disease - Rare immune disease - Rare infectious disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

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

	External references: No OMIM references No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.